Antireflux Suture In One Anastomsis Gastric Bypass
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorKhyber Teaching Hospital
About this trial
To prevent refulx symptoms in a type of bariatric surgery, a suture is taken.there is no enough evidence in support of or against the suture. our study aims to compare the symptoms of patients in whom the suture is taken and in those in whom it is not.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients undergoing one anastomosis gastric bypass surgery
Disqualifiers
Non consenting individuals
Trial design
Design model
Parallel
Treatments tested in this trial
Antireflux suture
Procedure/SurgeryAntireflux suture will be taken in this intervention group
No Antireflux suture
Procedure/SurgeryAntireflux suture will not be taken in this intervention group
Treatment groups
316 Participants
are divided into 2 treatment groupsGroup A: Antireflux suture groupExperimental treatment 1 intervention
Group B: No Antireflux sutureExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Reflux disease
The incidence of gastroesophageal reflux will be measured after surgery
Time frame
3 months and 6 months postoperativelySecondary outcomes
1
Postoperative vomiting
Incidence of postoperative vomiting will be measured
Time frame
At 3 months and 6 months postoperativelySponsors and contacts
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Source ClinicalTrials.gov