# Seprafilm Slurry in the Prevention of Uterine Scarring in Patients Undergoing Hysteroscopic Myomectomy

> **NCT01632202** · PHASE4 · TERMINATED · sponsor: **Weill Medical College of Cornell University** · enrollment: 11 (actual)

## Conditions studied

- Intrauterine Adhesions

## Interventions

- **DEVICE:** Seprafilm
- **DEVICE:** Sterile Saline Solution

## Key facts

- **NCT ID:** NCT01632202
- **Lead sponsor:** Weill Medical College of Cornell University
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2012-05
- **Primary completion:** 2014-01
- **Final completion:** 2014-01
- **Target enrollment:** 11 (ACTUAL)
- **Why stopped:** No subjects were recruited at the Weill Cornell site.
- **Last updated:** 2020-12-03

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01632202

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01632202, "Seprafilm Slurry in the Prevention of Uterine Scarring in Patients Undergoing Hysteroscopic Myomectomy". Retrieved via AI Analytics 2026-06-01 from https://api.ai-analytics.org/clinical/NCT01632202. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
