Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
200 participants
INTERVENTIONAL
2016-11-30
2017-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Single Anastomosis Sleeve Jejunal (SAS-J) Bypass
Single Anastomosis Sleeve Jejunal (SAS-J) Bypass as A treatment for Morbid
Single Anastomosis Sleeve Jejunal (SAS-J) Bypass
Single Anastomosis Sleeve Jejunal (SAS-J) Bypass as A treatment for Morbid
Interventions
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Single Anastomosis Sleeve Jejunal (SAS-J) Bypass
Single Anastomosis Sleeve Jejunal (SAS-J) Bypass as A treatment for Morbid
Eligibility Criteria
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Inclusion Criteria
* patients fit for laparoscopic surgery
* give approval to share in the study
Exclusion Criteria
* patients unfit for surgery
* patients aged less than 18 and older than 50
* patients with BMI less than 50
* patient with previous upper abdominal surgery either for obesity or other diseases
* patients with preoperative GERD clinically or by investigation
18 Years
50 Years
ALL
No
Sponsors
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Minia University
OTHER
Responsible Party
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Alaa Mstafa Hassan Sewefy
MD, Lecturer & consultant of general surgery, Department of surgery, Minia university hospital, Egypt
Principal Investigators
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Alaa M Sewefy, MD
Role: STUDY_CHAIR
Lecturer & consultant of general surgery, Department of surgery, Minia university hospital, Egypt.
Locations
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Minia university hospital
Minya, , Egypt
Countries
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Other Identifiers
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fac.med.016
Identifier Type: -
Identifier Source: org_study_id
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