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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04826055
Other study ID # fac.med 21.17
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 25, 2021
Est. completion date March 25, 2022

Study information

Verified date May 2022
Source Minia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

in all loop bypass bariatric procedure (mini gastric bypass & single anastomosis sleeve jejunal bypass), biliary limb is fixed length. we do it as a percentage from total small intestine length rather than fixed length


Description:

in all loop bypass bariatric procedure (mini gastric bypass & single anastomosis sleeve jejunal bypass), biliary limb is fixed length we count the length of small intestine and do it as a percentage from total small intestine length rather than fixed length


Recruitment information / eligibility

Status Completed
Enrollment 210
Est. completion date March 25, 2022
Est. primary completion date March 25, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - obese patients with BMI more than 40 or more than 35 with comorbidity - patients fit for laparoscopic surgery - give approval to share in the study Exclusion Criteria: - patients refused to share in the study - patients unfit for surgery - patients aged less than 18 and older than 50 - patients with BMI less than 35 - patient with previous upper abdominal surgery either for obesity or other diseases

Study Design


Related Conditions & MeSH terms


Intervention

Other:
biliary limb as fixed length
n all loop bypass procedures we will don't count the total length of small intestine and make the biliary limb as a fixed from total small intestine length as mentioned in literature
biliary limb as a percentage from small intestine length
in all loop bypass procedures we count the total length of small intestine and make the biliary limb as a percentage from total small intestine length rather than fixed length

Locations

Country Name City State
Egypt Faculty of medicine Minya

Sponsors (1)

Lead Sponsor Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary effect on weight loss the effect on weight loss one year
Primary effect on nutritional deficiency the effect on nutritional deficiency 1 year
Secondary operative time operative time from skin incision to skin closure 6 hours
Secondary effect on obesity comorbidities the effect on improvement of obesity related comorbidities 1 year
Secondary early complications the operative and postoperative 30 days complications 30 days
Secondary late complications the late reported complications 1 year
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