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OpenTrials
Completed

NCT Number: NCT00793728

Prospective Randomized Trial Comparing Two Techniques of Sleeve Gastrectomy

This study compares if there is any difference doing antrectomy while performing a sleeve gastrectomy for treating morbid obesity. The investigators compare the differences between leaving or not leaving the antrum in terms of food tolerance, weight lost and quality of life.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Universitari de Bellvitge

L'Hospitalet de Llobregat, Barcelona, 08907, Spain

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • BMI>40 kg/m2
  • Age >18 years old
  • Eligible for laparoscopic surgery

Exclusion criteria

  • Prior bariatric surgery
  • Sleeve gastrectomy as a part of a duodenal switch
  • Second time surgery before 18 months
  • Other procedures done during the surgery
  • Conversion to laparotomy

Treatment and study plan

Sleeve gastrectomy

Procedure

Perform a gastrectomy guided by a 38F catheter and parallel to the small curvature of the stomach

Primary outcomes

  1. Weight lose

    Time frame: One year

  2. Food tolerance

    Time frame: One year

  3. Quality of life

    Time frame: One year

Secondary outcomes

  1. Metabolic syndrome outcome

    Time frame: One year

Sponsors and collaborators

Lead sponsor

Hospital Universitari de Bellvitge

Other

Registry information

Important dates

Study start
2008
Primary completion
2015
Study completion
2015
First posted
Nov 19, 2008
Registry last updated
Aug 20, 2015

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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