To Assess the Anti-adhesive Effect and Safety of Protescal

Laparoscopic Myomectomy Clinical Trial

Official title:
To Assess the Anti-adhesive Effect and Safety of Protescal Following Laparoscopic Surgery

Status Terminated

Clinical Trial Summary

This multicenter, randomized, single-blind study assessed the safety and efficacy of Protescal for the reduction of post-operative adhesion formation following myomectomy.

Clinical Trial Description

The age of the patients participating in the study overed 20 years and included nonpregnant women requiring laparoscopic myomectomy and expected to undergo a second-look laparoscopy as part of their treatment plan 5 weeks after the initial surgery. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

Laparoscopic Myomectomy

Clinical Trial Details

NCT number	NCT01810900
Study type	Interventional
Source	LG Life Sciences
Contact
Status	Terminated
Phase	Phase 3
Start date	September 2012
Completion date	December 2013

View Details

See also
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Completed	`NCT00624390` - Sepraspray™ Laparoscopic Myomectomy Study	N/A
Terminated	`NCT03935815` - Quadratus Lumborum Nerve Blocks for Myomectomies	Phase 1
Completed	`NCT01530802` - Temporary Clipping of the Uterine Arteries During Laparoscopic Myomectomy	N/A
Recruiting	`NCT05154279` - The Effect of Intramyometrial Injection of Terlipressin Versus Intramyometrial Injection of Carbitocin on Hemoglobin and Blood Loss During Laparoscopic Myomectomy Operations	N/A
Terminated	`NCT00672750` - A Retrospective Review Of Outcomes Following Laparoscopic Myomectomy	N/A