{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Prolapse%2C+Uterine&page=2",
    "query": {
      "condition": "Prolapse, Uterine",
      "page": 2
    },
    "page_size": 10
  },
  "pagination": {
    "page": 2,
    "page_size": 10,
    "total_count": 10,
    "total_pages": 1,
    "next_page_url": null,
    "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Prolapse%2C+Uterine&page=1&page_size=10"
  },
  "source": "remote",
  "last_synced_at": "2026-07-22T18:19:43.427Z",
  "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": "NCT04440475",
      "title": "Tap Block vs Conventional Pain Medication for Patients Undergoing Robotic Sacrocolpopexy",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Anesthesia, Local",
        "Prolapse",
        "Prolapse; Female",
        "Prolapse, Vaginal",
        "Prolapse; Vagina, Posthysterectomy",
        "Pain, Postoperative"
      ],
      "interventions": [
        {
          "name": "TAP block",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "ProMedica 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": 40,
      "start_date": "2020-06-28",
      "completion_date": "2022-01-30",
      "has_results": false,
      "last_update_posted_date": "2024-09-19",
      "last_synced_at": "2026-07-22T18:19:43.427Z",
      "location_count": 1,
      "location_summary": "Toledo, Ohio",
      "locations": [
        {
          "city": "Toledo",
          "state": "Ohio"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04440475"
    },
    {
      "nct_id": "NCT05063331",
      "title": "Patient-Centered Outcomes in the Surgical Treatment of Uterovaginal Prolapse",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Uterine Prolapse"
      ],
      "interventions": [
        {
          "name": "Minimally invasive supracervical hysterectomy and sacrocolpopexy (MI-SCH+SCP)",
          "type": "PROCEDURE"
        },
        {
          "name": "Vaginal hysterectomy with uterosacral ligament suspension (TVH+USLS)",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "University Hospitals Cleveland Medical Center",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "80 Years",
        "sex": "FEMALE",
        "summary": "18 Years to 80 Years · Female only"
      },
      "enrollment_count": 300,
      "start_date": "2021-12-15",
      "completion_date": "2029-05-31",
      "has_results": false,
      "last_update_posted_date": "2026-05-15",
      "last_synced_at": "2026-07-22T18:19:43.427Z",
      "location_count": 7,
      "location_summary": "Jacksonville, Florida • Chicago, Illinois • Durham, North Carolina + 2 more",
      "locations": [
        {
          "city": "Jacksonville",
          "state": "Florida"
        },
        {
          "city": "Chicago",
          "state": "Illinois"
        },
        {
          "city": "Durham",
          "state": "North Carolina"
        },
        {
          "city": "Cleveland",
          "state": "Ohio"
        },
        {
          "city": "Cleveland",
          "state": "Ohio"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05063331"
    },
    {
      "nct_id": "NCT02888093",
      "title": "A Randomized Controlled Trial of Permanent vs Absorbable Suture for Uterosacral Ligament Suspension",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Pelvic Organ Prolapse",
        "Cystocele",
        "Uterine Prolapse"
      ],
      "interventions": [
        {
          "name": "Absorbent suture (polydioxanone) and Permanent suture (Gore-Tex CV2)",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Joseph Kowalski",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "99 Years",
        "sex": "FEMALE",
        "summary": "18 Years to 99 Years · Female only"
      },
      "enrollment_count": 44,
      "start_date": "2016-10",
      "completion_date": "2018-11",
      "has_results": true,
      "last_update_posted_date": "2019-12-02",
      "last_synced_at": "2026-07-22T18:19:43.427Z",
      "location_count": 1,
      "location_summary": "Iowa City, Iowa",
      "locations": [
        {
          "city": "Iowa City",
          "state": "Iowa"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02888093"
    },
    {
      "nct_id": "NCT03436979",
      "title": "The NeuGuide™ System for Vaginal Colpopexy in the Treatment of Uterine Prolapse",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Uterine Prolapse Without Vaginal Wall Prolapse"
      ],
      "interventions": [
        {
          "name": "NeuGuide™ System",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Pop Medical Solutions",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "36 Years",
        "maximum_age": "84 Years",
        "sex": "FEMALE",
        "summary": "36 Years to 84 Years · Female only"
      },
      "enrollment_count": 60,
      "start_date": "2018-01-01",
      "completion_date": "2023-10-31",
      "has_results": false,
      "last_update_posted_date": "2025-08-07",
      "last_synced_at": "2026-07-22T18:19:43.427Z",
      "location_count": 11,
      "location_summary": "Washington D.C., District of Columbia • Fort Lauderdale, Florida • Weston, Florida + 8 more",
      "locations": [
        {
          "city": "Washington D.C.",
          "state": "District of Columbia"
        },
        {
          "city": "Fort Lauderdale",
          "state": "Florida"
        },
        {
          "city": "Weston",
          "state": "Florida"
        },
        {
          "city": "Cambridge",
          "state": "Massachusetts"
        },
        {
          "city": "Brooklyn",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03436979"
    },
    {
      "nct_id": "NCT00557882",
      "title": "Efficacy Study of Vaginal Mesh for Anterior Prolapse",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Vaginal Prolapse",
        "Uterine Prolapse",
        "Cystocele",
        "Pelvic Organ Prolapse"
      ],
      "interventions": [
        {
          "name": "synthetic polypropylene mesh",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Medstar Health Research Institute",
      "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": 65,
      "start_date": "2007-06",
      "completion_date": "2011-11",
      "has_results": true,
      "last_update_posted_date": "2020-10-30",
      "last_synced_at": "2026-07-22T18:19:43.427Z",
      "location_count": 1,
      "location_summary": "Washington D.C., District of Columbia",
      "locations": [
        {
          "city": "Washington D.C.",
          "state": "District of Columbia"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00557882"
    },
    {
      "nct_id": "NCT04172896",
      "title": "Intraperitoneal and Extraperitoneal Uterosacral Ligament Suspensions for Post-Hysterectomy Vaginal Vault Prolapse",
      "overall_status": "UNKNOWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Vaginal Vault Prolapse",
        "Post-Hysterectomy Vaginal Vault Prolapse",
        "Prolapse, Vaginal"
      ],
      "interventions": [
        {
          "name": "Intraperitoneal Uterosacral Ligament Suspension",
          "type": "PROCEDURE"
        },
        {
          "name": "Extraperitoneal Uterosacral Ligament Suspension",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "The Methodist Hospital Research Institute",
      "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": 34,
      "start_date": "2019-11-01",
      "completion_date": "2021-09",
      "has_results": false,
      "last_update_posted_date": "2019-11-21",
      "last_synced_at": "2026-07-22T18:19:43.427Z",
      "location_count": 1,
      "location_summary": "Houston, Texas",
      "locations": [
        {
          "city": "Houston",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04172896"
    },
    {
      "nct_id": "NCT07120945",
      "title": "Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace Gynecology)",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Uterine Fibroids (UF)",
        "Menstrual Disorders",
        "Adenomyosis of Uterus",
        "Endometriosis",
        "Uterine Prolapse",
        "Precancerous/Nonmalignant Condition",
        "Cervical Cancer",
        "Endometrial Cancer",
        "Ovarian Cancer"
      ],
      "interventions": [
        {
          "name": "Robotic Assisted-Surgery (RAS) Hysterectomy",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Medtronic - MITG",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "22 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "22 Years and older · Female only"
      },
      "enrollment_count": 70,
      "start_date": "2025-08-28",
      "completion_date": "2031-05",
      "has_results": false,
      "last_update_posted_date": "2026-06-02",
      "last_synced_at": "2026-07-22T18:19:43.427Z",
      "location_count": 5,
      "location_summary": "Jacksonville, Florida • Tampa, Florida • Durham, North Carolina + 2 more",
      "locations": [
        {
          "city": "Jacksonville",
          "state": "Florida"
        },
        {
          "city": "Tampa",
          "state": "Florida"
        },
        {
          "city": "Durham",
          "state": "North Carolina"
        },
        {
          "city": "Pittsburgh",
          "state": "Pennsylvania"
        },
        {
          "city": "Seattle",
          "state": "Washington"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT07120945"
    },
    {
      "nct_id": "NCT01190618",
      "title": "Surgical Outcomes of Vaginal Prolapse Repair With Elevate",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Vaginal Prolapse"
      ],
      "interventions": [],
      "intervention_types": [],
      "sponsor": "Larry Sirls",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": null,
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "Female only"
      },
      "enrollment_count": 417,
      "start_date": "2010-08",
      "completion_date": "2016-12-31",
      "has_results": false,
      "last_update_posted_date": "2017-02-16",
      "last_synced_at": "2026-07-22T18:19:43.427Z",
      "location_count": 1,
      "location_summary": "Royal Oak, Michigan",
      "locations": [
        {
          "city": "Royal Oak",
          "state": "Michigan"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01190618"
    },
    {
      "nct_id": "NCT01802281",
      "title": "Study of Uterine Prolapse Procedures - Randomized Trial",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Uterovaginal Prolapse"
      ],
      "interventions": [
        {
          "name": "Uterosacral ligament suspension",
          "type": "PROCEDURE"
        },
        {
          "name": "Uphold® LITE",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "NICHD Pelvic Floor Disorders Network",
      "sponsor_class": "NETWORK",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "21 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "21 Years and older · Female only"
      },
      "enrollment_count": 183,
      "start_date": "2013-04-01",
      "completion_date": "2025-03-07",
      "has_results": true,
      "last_update_posted_date": "2025-08-26",
      "last_synced_at": "2026-07-22T18:19:43.427Z",
      "location_count": 8,
      "location_summary": "Birmingham, Alabama • La Jolla, California • Albuquerque, New Mexico + 5 more",
      "locations": [
        {
          "city": "Birmingham",
          "state": "Alabama"
        },
        {
          "city": "La Jolla",
          "state": "California"
        },
        {
          "city": "Albuquerque",
          "state": "New Mexico"
        },
        {
          "city": "Durham",
          "state": "North Carolina"
        },
        {
          "city": "Cleveland",
          "state": "Ohio"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01802281"
    },
    {
      "nct_id": "NCT03664986",
      "title": "Pudendal Block Using Liposomal Bupivacaine vs. Standard Treatment During Sacrospinous Ligament Fixation",
      "overall_status": "UNKNOWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Vaginal Prolapse"
      ],
      "interventions": [
        {
          "name": "Liposomal Bupivacaine",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "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": 88,
      "start_date": "2018-09-24",
      "completion_date": "2021-12-01",
      "has_results": false,
      "last_update_posted_date": "2021-05-10",
      "last_synced_at": "2026-07-22T18:19:43.427Z",
      "location_count": 1,
      "location_summary": "Morristown, New Jersey",
      "locations": [
        {
          "city": "Morristown",
          "state": "New Jersey"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03664986"
    }
  ]
}