MedTrace Logo

Efficacy of Sprayable PEG Barrier in Gynecologic Laparoscopy

NCT01187680 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2010-12-29

No results posted yet for this study

Summary

The purpose of the study is to investigate whether sprayable PEG barrier is effective in reducing adhesions in laparoscopic gynecologic surgery.

Conditions

  • Postoperative Adhesion
  • Peritoneal Adhesion, Nos

Interventions

DEVICE

Spraygel

DEVICE

Control

Good surgical technique, no adhesion barrier

Sponsors & Collaborators

  • Onze Lieve Vrouwe Gasthuis

    collaborator OTHER

  • Radboud University Medical Center

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-10-31
Primary Completion
2004-04-30
Completion
2009-07-31

Countries

  • Netherlands

Study Locations

More Related Trials

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 NCT01187680 on ClinicalTrials.gov