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Single Anastomosis Sleeve Jejunal Bypass as a Revisional Bariatric Procedure

Primary Purpose

Obesity, Morbid

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
SAS-J
Sponsored by
Minia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity, Morbid

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

obese patients with BMI more than 40 with or without co-morbidity or more than 35 with co-morbidity

  • patients fit for laparoscopic surgery
  • give approval to share in the study
  • previous restrictive bariatric procedure

Exclusion Criteria:

  • patients unfit for surgery
  • patients aged less than 18 and older than 60
  • patient with previous upper abdominal surgery either for obesity or other diseases

Sites / Locations

  • Minia university hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

SAS-J

Arm Description

single anastomosis sleeve Jejunal Bypass as a revisional bariatric procedure after restrictive bariatric procedures

Outcomes

Primary Outcome Measures

weight loss
percentage of excess weight loss in kilogram

Secondary Outcome Measures

the rate of improved co morbidity
the effect of the operation on co morbidity like diabetes and hypertension the effect of the operation on co morbidity like diabetes and hypertension the effect of single anastomosis sleeve jejunal bypass of comorbidities
the incidence of nutritional deficiency
the incidence of nutritional deficiency like anemia, hypocalcamia, hypoproteinemia. the incidence of nutritional deficiency like ca, iron, vitaminD and protein malnutrition
the incidence of early operative complications the incidence of early operative complications the incidence of early operative complications the incidence of complications
early operative complications like leak, bleeding complications like leak, bleeding, dumping,

Full Information

First Posted
February 25, 2022
Last Updated
February 25, 2022
Sponsor
Minia University
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1. Study Identification

Unique Protocol Identification Number
NCT05269420
Brief Title
Single Anastomosis Sleeve Jejunal Bypass as a Revisional Bariatric Procedure
Official Title
Single Anastomosis Sleeve Jejunal Bypass as a Revisional Operation After Restrictive Bariatric Proceures
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
January 12, 2017 (Actual)
Primary Completion Date
December 8, 2020 (Actual)
Study Completion Date
January 4, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Minia University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
single anastomosis sleeve jejunal bypass as a revisional procedure after weight regain or failure after laparoscopic sleeve gastrectomy, gastric plications or laparoscopic adjustable gastric band
Detailed Description
in this study the investigators aim to test the efficacy of single anastomosis sleeve jejunal bypass as a revisional procedure after weight regain or failure after laparoscopic sleeve gastrectomy, gastric plications or laparoscopic adjustable gastric band

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Morbid

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
43 (Actual)

8. Arms, Groups, and Interventions

Arm Title
SAS-J
Arm Type
Experimental
Arm Description
single anastomosis sleeve Jejunal Bypass as a revisional bariatric procedure after restrictive bariatric procedures
Intervention Type
Procedure
Intervention Name(s)
SAS-J
Intervention Description
Single Anastomosis Sleeve Jejunal Bypass
Primary Outcome Measure Information:
Title
weight loss
Description
percentage of excess weight loss in kilogram
Time Frame
12 months
Secondary Outcome Measure Information:
Title
the rate of improved co morbidity
Description
the effect of the operation on co morbidity like diabetes and hypertension the effect of the operation on co morbidity like diabetes and hypertension the effect of single anastomosis sleeve jejunal bypass of comorbidities
Time Frame
12 months
Title
the incidence of nutritional deficiency
Description
the incidence of nutritional deficiency like anemia, hypocalcamia, hypoproteinemia. the incidence of nutritional deficiency like ca, iron, vitaminD and protein malnutrition
Time Frame
12-24 months
Title
the incidence of early operative complications the incidence of early operative complications the incidence of early operative complications the incidence of complications
Description
early operative complications like leak, bleeding complications like leak, bleeding, dumping,
Time Frame
12-24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: obese patients with BMI more than 40 with or without co-morbidity or more than 35 with co-morbidity patients fit for laparoscopic surgery give approval to share in the study previous restrictive bariatric procedure Exclusion Criteria: patients unfit for surgery patients aged less than 18 and older than 60 patient with previous upper abdominal surgery either for obesity or other diseases
Facility Information:
Facility Name
Minia university hospital
City
Minya
ZIP/Postal Code
61511
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Single Anastomosis Sleeve Jejunal Bypass as a Revisional Bariatric Procedure

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