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Not listed Phase 1Phase 2 Interventional Accepts healthy volunteers

Flat Polypropylene Mesh in the Treatment of Uterine and Recurrent or Advanced Pelvic Organ Prolapse

ClinicalTrials.gov ID: NCT06225375

Public ClinicalTrials.gov record NCT06225375. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 11:07 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Prospective Analysis of Flat Polypropylene Mesh in the Treatment of Uterine (by Uterine-sparing Hysteropexy) and Recurrent or Advanced Pelvic Organ Prolapse: a Safety and Feasibility Study

Study identification

NCT ID
NCT06225375
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Michigan Institution of Women's Health PC
Other
Enrollment
30 participants

Conditions and interventions

Interventions

  • Restorelle® Flat Mesh Device

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2021
Primary completion
Nov 30, 2025
Completion
Dec 31, 2025
Last update posted
Jan 24, 2024

2021 – 2026

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Michigan Women's Institution of Health PC. Dearborn Michigan 48124

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06225375, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 24, 2024 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06225375 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →