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Assessment of Uterine Access, Uterine Patency and Intrauterine Adhesions Following Endometrial Ablation

NCT04824430 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 36

Last updated 2022-06-16

No results posted yet for this study

Summary

The objective of this study is to gain information concerning the acute and longer-term morphological changes within the uterus following endometrial ablation. Hysteroscopic evaluation of the uterine cavity will be used to determine if physical access and the ability to systematically assess the post-ablation uterine cavity were preserved. The presence, location and severity of intrauterine adhesions will be documented in participants who are 3, 6 and 12 months from their standard of care endometrial ablation.

Conditions

  • Intrauterine Adhesion

Sponsors & Collaborators

  • Rejoni Inc.

    lead INDUSTRY

Principal Investigators

  • Cindy Basinski, MD · Basinski and Juran MDs

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-03-23
Primary Completion
2021-07-22
Completion
2021-07-22

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04824430 on ClinicalTrials.gov