{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Cystocele",
    "query": {
      "condition": "Cystocele"
    },
    "page_size": 10
  },
  "pagination": {
    "page": 1,
    "page_size": 10,
    "total_count": 21,
    "total_pages": 3,
    "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Cystocele&page=2&page_size=10",
    "previous_page_url": null
  },
  "source": "remote",
  "last_synced_at": "2026-05-22T04:19:44.298Z",
  "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": "NCT01393171",
      "title": "Anterior Colporrhaphy Versus Cystocele Repair Using Polypropylene Mesh or Porcine Dermis",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Anterior Vaginal Wall Prolapse",
        "Cystocele",
        "Pelvic Organ Prolapse"
      ],
      "interventions": [
        {
          "name": "Polypropylene mesh (Polyform by Boston Scientific)",
          "type": "DEVICE"
        },
        {
          "name": "Porcine Dermis (Pelvicol by CRBard)",
          "type": "PROCEDURE"
        },
        {
          "name": "Anterior Colporrhaphy",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "PROCEDURE"
      ],
      "sponsor": "Kaiser Permanente",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "18 Years and older · Female only"
      },
      "enrollment_count": 99,
      "start_date": "2006-01",
      "completion_date": "2018-04-01",
      "has_results": true,
      "last_update_posted_date": "2023-11-13",
      "last_synced_at": "2026-05-22T04:19:44.298Z",
      "location_count": 2,
      "location_summary": "Downey, California • San Diego, California",
      "locations": [
        {
          "city": "Downey",
          "state": "California"
        },
        {
          "city": "San Diego",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01393171"
    },
    {
      "nct_id": "NCT04038099",
      "title": "Lessons on Urethral Lidocaine in Urodynamics",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Urethra Issue",
        "Pelvic Organ Prolapse",
        "Urinary Incontinence",
        "Vaginal Vault Prolapse",
        "Cystocele",
        "Uterine Prolapse",
        "Vaginal Prolapse",
        "Pelvic Floor Disorders"
      ],
      "interventions": [
        {
          "name": "Water-Based Vaginal Lubricant",
          "type": "DRUG"
        },
        {
          "name": "lidocaine topical",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "University of Texas Southwestern Medical Center",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "18 Years and older · Female only"
      },
      "enrollment_count": 63,
      "start_date": "2019-08-14",
      "completion_date": "2021-08-18",
      "has_results": true,
      "last_update_posted_date": "2023-08-01",
      "last_synced_at": "2026-05-22T04:19:44.298Z",
      "location_count": 1,
      "location_summary": "Dallas, Texas",
      "locations": [
        {
          "city": "Dallas",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04038099"
    },
    {
      "nct_id": "NCT00535301",
      "title": "Outcomes of Anterior Colporrhaphy Versus Graft Reinforced Anterior Prolapse Repair",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Cystocele",
        "Uterine Prolapse",
        "Urinary Incontinence"
      ],
      "interventions": [
        {
          "name": "grafted anterior prolapse repair",
          "type": "DEVICE"
        },
        {
          "name": "sutured anterior vaginal prolapse repair",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "PROCEDURE"
      ],
      "sponsor": "Kaiser Permanente",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "21 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "21 Years and older · Female only"
      },
      "enrollment_count": 75,
      "start_date": "2005-01",
      "completion_date": "2008-04",
      "has_results": true,
      "last_update_posted_date": "2015-04-22",
      "last_synced_at": "2026-05-22T04:19:44.298Z",
      "location_count": 1,
      "location_summary": "Downey, California",
      "locations": [
        {
          "city": "Downey",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00535301"
    },
    {
      "nct_id": "NCT00774215",
      "title": "Evaluation of the Avaulta Procedure for the Correction of Pelvic Organ Prolapse - Results at 1 Year",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Pelvic Organ Prolapse"
      ],
      "interventions": [],
      "intervention_types": [],
      "sponsor": "Atlantic Health System",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "18 Years and older · Female only"
      },
      "enrollment_count": 103,
      "start_date": "2007-10",
      "completion_date": "2009-04",
      "has_results": false,
      "last_update_posted_date": "2010-01-26",
      "last_synced_at": "2026-05-22T04:19:44.298Z",
      "location_count": 1,
      "location_summary": "Morristown, New Jersey",
      "locations": [
        {
          "city": "Morristown",
          "state": "New Jersey"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00774215"
    },
    {
      "nct_id": "NCT02162615",
      "title": "Restorelle® Mesh Versus Native Tissue Repair for Prolapse",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Pelvic Organ Prolapse"
      ],
      "interventions": [
        {
          "name": "Restorelle Direct Fix A",
          "type": "DEVICE"
        },
        {
          "name": "Restorelle Direct Fix P",
          "type": "DEVICE"
        },
        {
          "name": "Native Tissue Repair Anterior",
          "type": "PROCEDURE"
        },
        {
          "name": "Native Tissue Repair Posterior",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "PROCEDURE"
      ],
      "sponsor": "Coloplast A/S",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "18 Years and older · Female only"
      },
      "enrollment_count": 810,
      "start_date": "2014-08",
      "completion_date": "2021-11-06",
      "has_results": false,
      "last_update_posted_date": "2022-01-27",
      "last_synced_at": "2026-05-22T04:19:44.298Z",
      "location_count": 33,
      "location_summary": "Agoura Hills, California • Stanford, California • Denver, Colorado + 30 more",
      "locations": [
        {
          "city": "Agoura Hills",
          "state": "California"
        },
        {
          "city": "Stanford",
          "state": "California"
        },
        {
          "city": "Denver",
          "state": "Colorado"
        },
        {
          "city": "New Haven",
          "state": "Connecticut"
        },
        {
          "city": "Newark",
          "state": "Delaware"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02162615"
    },
    {
      "nct_id": "NCT02431897",
      "title": "Investigation to Minimize Prolapse Recurrence of the Vagina Using Estrogen",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Pelvic Organ Prolapse",
        "Urogenital Prolapse",
        "Vaginal Vault Prolapse",
        "Cystocele",
        "Uterine Prolapse",
        "Vaginal Prolapse",
        "Pelvic Floor Disorders"
      ],
      "interventions": [
        {
          "name": "Conjugated Estrogens Cream",
          "type": "DRUG"
        },
        {
          "name": "Placebo Cream",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "University of Texas Southwestern Medical Center",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "48 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "48 Years and older · Female only"
      },
      "enrollment_count": 206,
      "start_date": "2016-12",
      "completion_date": "2023-05-17",
      "has_results": true,
      "last_update_posted_date": "2023-09-06",
      "last_synced_at": "2026-05-22T04:19:44.298Z",
      "location_count": 3,
      "location_summary": "Birmingham, Alabama • Providence, Rhode Island • Dallas, Texas",
      "locations": [
        {
          "city": "Birmingham",
          "state": "Alabama"
        },
        {
          "city": "Providence",
          "state": "Rhode Island"
        },
        {
          "city": "Dallas",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02431897"
    },
    {
      "nct_id": "NCT02800512",
      "title": "SCP vs HUSLS for Pelvic Organ Prolapse Repair",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Pelvic Organ Prolapse",
        "Cystocele",
        "Rectocele",
        "Enterocele"
      ],
      "interventions": [
        {
          "name": "Robotic sacrocolpopexy",
          "type": "PROCEDURE"
        },
        {
          "name": "high uterosacral ligament suspension",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Loma Linda University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "100 Years",
        "sex": "FEMALE",
        "summary": "18 Years to 100 Years · Female only"
      },
      "enrollment_count": 112,
      "start_date": "2016-12",
      "completion_date": "2025-12",
      "has_results": false,
      "last_update_posted_date": "2025-01-03",
      "last_synced_at": "2026-05-22T04:19:44.298Z",
      "location_count": 1,
      "location_summary": "Loma Linda, California",
      "locations": [
        {
          "city": "Loma Linda",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02800512"
    },
    {
      "nct_id": "NCT00388947",
      "title": "Observational Data Collection of Surgical Outcomes in the Treatment of Vaginal Prolapse With AMS Products",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Vaginal Prolapse"
      ],
      "interventions": [
        {
          "name": "AMS Prolapse Product",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "ASTORA Women's Health",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "21 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "21 Years and older · Female only"
      },
      "enrollment_count": 1543,
      "start_date": "2006-09",
      "completion_date": "2010-05",
      "has_results": true,
      "last_update_posted_date": "2016-08-11",
      "last_synced_at": "2026-05-22T04:19:44.298Z",
      "location_count": 1,
      "location_summary": "Whitinsville, Massachusetts",
      "locations": [
        {
          "city": "Whitinsville",
          "state": "Massachusetts"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00388947"
    },
    {
      "nct_id": "NCT00223106",
      "title": "Treatment for Stress and Mixed Urinary Incontinence and Vaginal Vault Prolapse",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Urinary Incontinence, Stress",
        "Mixed Incontinence",
        "Vaginal Vault Prolapse"
      ],
      "interventions": [
        {
          "name": "Vaginal Sling",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Medtronic - MITG",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "18 Years and older · Female only"
      },
      "enrollment_count": 467,
      "start_date": "2004-03",
      "completion_date": "2007-09",
      "has_results": false,
      "last_update_posted_date": "2015-07-27",
      "last_synced_at": "2026-05-22T04:19:44.298Z",
      "location_count": 1,
      "location_summary": "Norwalk, Connecticut",
      "locations": [
        {
          "city": "Norwalk",
          "state": "Connecticut"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00223106"
    },
    {
      "nct_id": "NCT07544667",
      "title": "Poly-L-Lactic Acid for Vulvovaginal Tissue Regeneration",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Pelvic Organ Prolapse (POP)",
        "Cystocele",
        "Pelvic Floor Disorder"
      ],
      "interventions": [
        {
          "name": "Poly-L-Lactic Acid (Sculptra) injection",
          "type": "DEVICE"
        },
        {
          "name": "Placebo injection (sterile water)",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "OTHER"
      ],
      "sponsor": "Cassandra Kisby",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "21 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "21 Years and older · Female only"
      },
      "enrollment_count": 20,
      "start_date": "2026-05",
      "completion_date": "2028-06",
      "has_results": false,
      "last_update_posted_date": "2026-04-24",
      "last_synced_at": "2026-05-22T04:19:44.298Z",
      "location_count": 1,
      "location_summary": "Durham, North Carolina",
      "locations": [
        {
          "city": "Durham",
          "state": "North Carolina"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT07544667"
    }
  ]
}