Single Anastomosis Sleeve Jejunal (SAS-J) Bypass

NCT ID: NCT02870530

Last Updated: 2022-03-11

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-11-30

Study Completion Date

2017-04-30

Brief Summary

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The purpose of this study is to determine the efficacy of single anastomoses sleeve jejunal bypass as a treatment for morbid obesity

Detailed Description

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in this study the investigators aim to test a new technique ( single anastomoses sleeve jejunal as a treatment for morbid obesity Which is a modification of Single anastomoses sleeve ileal bypass with short biliary limb ( about one third of the small intestine from the Duodeno-jejunal junction

Conditions

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Morbid Obesity

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

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

Group Type EXPERIMENTAL

Single Anastomosis Sleeve Jejunal (SAS-J) Bypass

Intervention Type PROCEDURE

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

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* obese patients with BMI more than 40
* 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 50
* patient with previous upper abdominal surgery either for obesity or other diseases
* patients with preoperative GERD clinically or by investigation
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Minia University

OTHER

Sponsor Role lead

Responsible Party

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Alaa Mstafa Hassan Sewefy

MD, Lecturer & consultant of general surgery, Department of surgery, Minia university hospital, Egypt

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status

Countries

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Egypt

Other Identifiers

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fac.med.016

Identifier Type: -

Identifier Source: org_study_id

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