ClinicalTrials.gov record
Completed Phase 3 Interventional

Safety and Effectiveness of Juveena™ Hydrogel System Following Transcervical Gynecologic Procedures (TCGP) At High-Risk for Intrauterine Adhesions

ClinicalTrials.gov ID: NCT05394662

Public ClinicalTrials.gov record NCT05394662. 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 May 20, 2026, 10:41 AM EDT

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

Official title

Safety and Effectiveness of Juveena™ Hydrogel System Following Transcervical Gynecologic Procedures (TCGP) At High-Risk for Intrauterine Adhesions: A Multicenter Randomized Controlled Subject and Evaluator Blinded Pivotal Study

Study identification

NCT ID
NCT05394662
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Rejoni Inc.
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

  • Juveena Hydrogel System Device
  • Transcervical Gynecologic Procedures (TCGP) Procedure

Device · Procedure

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Aug 10, 2022
Primary completion
Apr 22, 2025
Completion
Apr 22, 2025
Last update posted
Apr 20, 2026

2022 – 2025

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Arizona Gynecology Consultants Phoenix Arizona 85020
UCSF Center for Reproductive Health San Francisco California 94158
MedStar Washington Hospital Center Washington D.C. District of Columbia 20010
Dr. Charles Miller and Associates Park Ridge Illinois 60068
Cypress Medical Research Center Wichita Kansas 67226
Newton Wellesley Hospital Newton Massachusetts 02462
Boston IVF Waltham Massachusetts 02451
Maimonides Medical Center Brooklyn New York 11219
Duke Universtiy Health System Morrisville North Carolina 27560
University Hospitals Landerbrook Mayfield Heights Ohio 41124
Prisma Health, Greensville Memorial Hospital Greenville South Carolina 29605
The University of Texas at Austin Dept of Womens' Health Austin Texas 78712
Texas Fertility Center Austin Texas 78731
Aspire Houston Fertility Institute Houston Texas 77063
Generations Fertility Care Middleton Wisconsin 53562

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 NCT05394662, 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 Apr 20, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05394662 live on ClinicalTrials.gov.

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