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NCT03485859: BELT

Effect of Abdominal Binder aftEr Laparoscopic Treatment on Postoperative Recovery

Completed NA Last updated 3 April 2019
What this trial tests

NA trial testing Experimental group in Laparoscopy in 66 participants. Completed in 31 October 2018.

Timeline
20 April 2018
Primary endpoint
5 August 2018
31 October 2018

Quick facts

Lead sponsorKangbuk Samsung Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment66
Start date20 April 2018
Primary completion5 August 2018
Estimated completion31 October 2018
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Kangbuk Samsung Hospital

Who can join

Adults 18 to 65, female only, with Laparoscopy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

There have been no studies exploring the efficacy of incision support using an elastic abdominal binder after laparoscopy to date. The investigators performed therefore a randomized controlled trial to determine the effect of post-laparoscopic abdominal binder use on enhanced recovery after surgery (ERAS) in patients with gynecologic disease.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Experimental group

Trials testing the same drug.

Other recruiting trials for Laparoscopy

Currently open trials in the same condition.

Other Kangbuk Samsung Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03485859.

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