A Clinical Intervention Study Exploring Gastropexy as a Measure to Reduce Gastro-oesophageal Reflux Disease After Laparoscopic Sleeve Gastrectomy

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to test gastropexy as a measure to reduce reflux in morbidly obese patients being submitted to sleeve gastrectomy. The main questions it aims to answer are: Does gastropexy reduce reflux symptoms? Does gastropexy reduce objective evidence of reflux? Participants will be randomized to gastropexy or no gastropexy, and researchers will compare these groups to see if reflux (symptoms / objective evidence of) is different in the two groups.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients planned for bariatric surgery with primary LSG

Locations
Other Locations
Norway
Helse Forde
NOT_YET_RECRUITING
Førde
Aleris Oslo
RECRUITING
Oslo
Volda sjukehus
RECRUITING
Volda
Voss sjukehus
RECRUITING
Voss
Contact Information
Primary
Villy Vage, MD PhD
villy.vage@helse-bergen.no
47 90863744
Backup
John Andersen, PhD
john.roger.andersen@helse-forde.no
47 48278186
Time Frame
Start Date: 2023-09-04
Estimated Completion Date: 2030-12
Participants
Target number of participants: 550
Treatments
Active_comparator: No gastropexy
Sleeve gastrectomy without gastropexy.
Experimental: Gastropexy
Sleeve gastrectomy with gastropexy
Sponsors
Leads: Helse Forde

This content was sourced from clinicaltrials.gov