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Completed

NCT Number: NCT02870530

Single Anastomosis Sleeve Jejunal (SAS-J) Bypass

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

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Key information

Conditions

Morbid Obesity Body Weight Nutrition Disorders Nutritional and Metabolic Diseases Obesity Obesity, Morbid Overnutrition Overweight Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Minia university hospital

Minya, 61511, Egypt

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Single Anastomosis Sleeve Jejunal (SAS-J) Bypass

Procedure

Single Anastomosis Sleeve Jejunal (SAS-J) Bypass as A treatment for Morbid

Primary outcomes

  1. operative time

    Time frame: the 1st 24 hours

    the operative time from skin incision to skin closure

  2. intraoperative complications

    Time frame: the 1st 24 hours

    intraoperative complications like bleeding, other organs injuries

  3. the postoperative weight loss

    Time frame: 12 month

    the percentage of weight loss from total excess body weight

Secondary outcomes

  1. effect on metabolic syndrome if present

    Time frame: 12 months

    effect on blood sugar level, blood pressure and blood cholesterol level

Other outcomes

  1. postoperative biliary reflux

    Time frame: 3 months

    the presence of postoperative biliary reflux clinically and by upper endoscopy

Sponsors and collaborators

Lead sponsor

Minia University

Other

Registry information

Official study title

Single Anastomosis Sleeve Jejunal (SAS-J) Bypass as A Treatment for Morbid Obesity

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Aug 17, 2016
Registry last updated
Mar 11, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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