{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Condom&page=6",
    "query": {
      "intervention": "Condom",
      "page": 6
    },
    "page_size": 10
  },
  "pagination": {
    "page": 6,
    "page_size": 10,
    "total_count": 470,
    "total_pages": 47,
    "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Condom&page=7&page_size=10",
    "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Condom&page=5&page_size=10"
  },
  "source": "remote",
  "last_synced_at": "2026-10-21T21:23:10.619Z",
  "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.",
  "notes": [
    "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.",
    "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.",
    "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees."
  ],
  "trials": [
    {
      "nct_id": "NCT01645033",
      "title": "Computer-based Cognitive Behavioral Therapy for Risky Behaviors in Opioid Dependent Patients",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Opioid Dependence",
        "Hepatitis",
        "HIV"
      ],
      "interventions": [
        {
          "name": "computerized Cognitive Behavioral Therapy (CBT)",
          "type": "OTHER"
        },
        {
          "name": "Treatment as Usual (TAU)",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "Yale University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 63,
      "start_date": "2012-04",
      "completion_date": "2013-12",
      "has_results": false,
      "last_update_posted_date": "2014-09-12",
      "last_synced_at": "2026-10-21T21:23:10.619Z",
      "location_count": 1,
      "location_summary": "Hartford, Connecticut",
      "locations": [
        {
          "city": "Hartford",
          "state": "Connecticut"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01645033"
    },
    {
      "nct_id": "NCT02419690",
      "title": "Sexual Health Texting Intervention to Support Adolescent Females",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Teen Sexual Health"
      ],
      "interventions": [
        {
          "name": "text message intervention",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "Denver Health and Hospital Authority",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "13 Years",
        "maximum_age": "18 Years",
        "sex": "FEMALE",
        "summary": "13 Years to 18 Years · Female only"
      },
      "enrollment_count": 244,
      "start_date": "2015-04",
      "completion_date": "2017-01",
      "has_results": true,
      "last_update_posted_date": "2020-11-10",
      "last_synced_at": "2026-10-21T21:23:10.619Z",
      "location_count": 1,
      "location_summary": "Denver, Colorado",
      "locations": [
        {
          "city": "Denver",
          "state": "Colorado"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02419690"
    },
    {
      "nct_id": "NCT05833048",
      "title": "Rectus Sheath Block in Cardiac Surgery",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Cardiac Disease",
        "Postoperative Pain"
      ],
      "interventions": [
        {
          "name": "Rectus sheath block",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Icahn School of Medicine at Mount Sinai",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "85 Years",
        "sex": "ALL",
        "summary": "18 Years to 85 Years"
      },
      "enrollment_count": 75,
      "start_date": "2024-07-29",
      "completion_date": "2026-12-31",
      "has_results": false,
      "last_update_posted_date": "2026-07-31",
      "last_synced_at": "2026-10-21T21:23:10.619Z",
      "location_count": 1,
      "location_summary": "New York, New York",
      "locations": [
        {
          "city": "New York",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05833048"
    },
    {
      "nct_id": "NCT03408743",
      "title": "Engineering an Online STI Prevention Program: CSE2",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Alcohol Consumption",
        "Sexually Transmitted Diseases"
      ],
      "interventions": [
        {
          "name": "Knowledge Alone",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Self-efficacy alone",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Perceived benefits alone",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Benefits and self-efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Injunctive norms alone",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Injunctive norms and self-efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Injunctive norms and benefits",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Injunctive norms, benefits, self-efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Descriptive norms alone",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Descriptive norms and self-efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Descriptive norms and perceived benefits",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Descriptive norms, benefits, self-efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Descriptive norms and injunctive norms",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Descriptive and injunctive norms, self-efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Descriptive and injunctive norms, and benefits",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Descriptive & injunctive norms, benefits, efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies alone",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies and self-efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies and perceived benefits",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, benefits, self-efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies and injunctive norms",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, injunctive norms, self-efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, injunctive norms, and benefits",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, injunctive norms, benefits, efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies and descriptive norms",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, descriptive norms, & self-efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, descriptive norms, benefits",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, descriptive norms, benefits, efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, descriptive and injunctive norms",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, descriptive & injunctive norms, efficacy",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, descriptive & injunctive norms, benefits",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Expectancies, descriptive & injunctive, benefits, efficacy",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "Penn State University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "30 Years",
        "sex": "ALL",
        "summary": "18 Years to 30 Years"
      },
      "enrollment_count": 2946,
      "start_date": "2017-09-18",
      "completion_date": "2017-12-31",
      "has_results": false,
      "last_update_posted_date": "2019-07-05",
      "last_synced_at": "2026-10-21T21:23:10.619Z",
      "location_count": 4,
      "location_summary": "Fresno, California • Fargo, North Dakota • Murfreesboro, Tennessee + 1 more",
      "locations": [
        {
          "city": "Fresno",
          "state": "California"
        },
        {
          "city": "Fargo",
          "state": "North Dakota"
        },
        {
          "city": "Murfreesboro",
          "state": "Tennessee"
        },
        {
          "city": "College Station",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03408743"
    },
    {
      "nct_id": "NCT01771237",
      "title": "HIV Prevention Among Vulnerable Male Youth",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Homosexuality, Male",
        "HIV",
        "Substance-related Disorders",
        "Sexual Dysfunctions, Psychological"
      ],
      "interventions": [
        {
          "name": "MyPeeps Manualized Group Intervention",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Standard Sexual Health Education",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "Ann & Robert H Lurie Children's Hospital of Chicago",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "16 Years",
        "maximum_age": "20 Years",
        "sex": "MALE",
        "summary": "16 Years to 20 Years · Male only"
      },
      "enrollment_count": 121,
      "start_date": "2007-07",
      "completion_date": "2011-01",
      "has_results": false,
      "last_update_posted_date": "2021-01-27",
      "last_synced_at": "2026-10-21T21:23:10.619Z",
      "location_count": 1,
      "location_summary": "Chicago, Illinois",
      "locations": [
        {
          "city": "Chicago",
          "state": "Illinois"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01771237"
    },
    {
      "nct_id": "NCT01898221",
      "title": "Vein of Marshall Ethanol Infusion for Persistent Atrial Fibrillation",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE3"
      ],
      "conditions": [
        "Ventricular Tachycardia",
        "Atrial Fibrillation"
      ],
      "interventions": [
        {
          "name": "Ethanol",
          "type": "DRUG"
        },
        {
          "name": "Ablation",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "DRUG",
        "PROCEDURE"
      ],
      "sponsor": "The Methodist Hospital Research Institute",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "85 Years",
        "sex": "ALL",
        "summary": "18 Years to 85 Years"
      },
      "enrollment_count": 343,
      "start_date": "2013-10",
      "completion_date": "2019-12",
      "has_results": true,
      "last_update_posted_date": "2025-08-21",
      "last_synced_at": "2026-10-21T21:23:10.619Z",
      "location_count": 12,
      "location_summary": "Phoenix, Arizona • Los Angeles, California • San Diego, California + 7 more",
      "locations": [
        {
          "city": "Phoenix",
          "state": "Arizona"
        },
        {
          "city": "Los Angeles",
          "state": "California"
        },
        {
          "city": "San Diego",
          "state": "California"
        },
        {
          "city": "Denver",
          "state": "Colorado"
        },
        {
          "city": "Atlanta",
          "state": "Georgia"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01898221"
    },
    {
      "nct_id": "NCT02466893",
      "title": "COMPASS Trial: a Direct Aspiration First Pass Technique",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Ischemic Cerebrovascular Accident"
      ],
      "interventions": [
        {
          "name": "Adapt/Standard Stent Retriever (SR) Group",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "Medical University of South Carolina",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 250,
      "start_date": "2015-06",
      "completion_date": "2018-02",
      "has_results": false,
      "last_update_posted_date": "2018-02-12",
      "last_synced_at": "2026-10-21T21:23:10.619Z",
      "location_count": 1,
      "location_summary": "Charleston, South Carolina",
      "locations": [
        {
          "city": "Charleston",
          "state": "South Carolina"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02466893"
    },
    {
      "nct_id": "NCT03522077",
      "title": "RAVE: Radial Artery Vascular Complication and Resource Utilization",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Angiogram",
        "Percutaneous Coronary Intervention"
      ],
      "interventions": [
        {
          "name": "RadAR EasyCLik plus ®-STF hemostatic pad",
          "type": "DEVICE"
        },
        {
          "name": "TR BAND® Compression device plus ®-STF hemostatic pad",
          "type": "DEVICE"
        },
        {
          "name": "SoftSeal®-STF hemostatic pad",
          "type": "DEVICE"
        },
        {
          "name": "VascBand™ Hemostat",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Wake Forest University Health Sciences",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 300,
      "start_date": "2018-05-09",
      "completion_date": "2021-12-01",
      "has_results": true,
      "last_update_posted_date": "2024-10-03",
      "last_synced_at": "2026-10-21T21:23:10.619Z",
      "location_count": 1,
      "location_summary": "Milwaukee, Wisconsin",
      "locations": [
        {
          "city": "Milwaukee",
          "state": "Wisconsin"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03522077"
    },
    {
      "nct_id": "NCT02851511",
      "title": "Augmenting Cognitive Training In Older Adults",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Aging"
      ],
      "interventions": [
        {
          "name": "Cognitive Training",
          "type": "BEHAVIORAL"
        },
        {
          "name": "tDCS (active stimulation)",
          "type": "DEVICE"
        },
        {
          "name": "tDCS (sham stimulation)",
          "type": "DEVICE"
        },
        {
          "name": "Educational Training",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL",
        "DEVICE"
      ],
      "sponsor": "University of Florida",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "65 Years",
        "maximum_age": "89 Years",
        "sex": "ALL",
        "summary": "65 Years to 89 Years"
      },
      "enrollment_count": 379,
      "start_date": "2017-08-08",
      "completion_date": "2022-04-30",
      "has_results": true,
      "last_update_posted_date": "2024-04-17",
      "last_synced_at": "2026-10-21T21:23:10.619Z",
      "location_count": 3,
      "location_summary": "Tucson, Arizona • Gainesville, Florida",
      "locations": [
        {
          "city": "Tucson",
          "state": "Arizona"
        },
        {
          "city": "Gainesville",
          "state": "Florida"
        },
        {
          "city": "Gainesville",
          "state": "Florida"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02851511"
    },
    {
      "nct_id": "NCT05368571",
      "title": "CHOICES-TEEN Randomized Controlled Trial",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Risk for an Alcohol-Exposed Pregnancy",
        "Risk for Marijuana-Exposed Pregnancy",
        "Risk for Substance-Exposed Pregnancy",
        "HIV Risk",
        "Sexually Transmitted Infection Risk"
      ],
      "interventions": [
        {
          "name": "CHOICES-TEEN",
          "type": "OTHER"
        },
        {
          "name": "Health and Life Skills Education",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "Danielle Parrish",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "14 Years",
        "maximum_age": "19 Years",
        "sex": "FEMALE",
        "summary": "14 Years to 19 Years · Female only"
      },
      "enrollment_count": 400,
      "start_date": "2022-04-08",
      "completion_date": "2027-02-28",
      "has_results": false,
      "last_update_posted_date": "2026-09-23",
      "last_synced_at": "2026-10-21T21:23:10.619Z",
      "location_count": 1,
      "location_summary": "Houston, Texas",
      "locations": [
        {
          "city": "Houston",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05368571"
    }
  ]
}