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OpenTrials
Completed

NCT Number: NCT04333979

The Effect of Drain Use on Patient Comfort in Laparoscopic Sleeve Gastrectomy

Introduction Laparoscopic sleeve gastrectomy surgeon; Have become increasingly morbid obesity treatment methods with improvements in minimally invasive surgery. Ensuring patient comfort and early return to life are the criteria that should be given priority in this treatment method. The purpose of this study is to determine the use of drain, which closely affects these criteria; And the effect on patient comfort.

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Key information

About this study

Question the necessity of routine use of drain in Laparoscopic sleeve gastrectomy surgeon

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Morbid obese patients

Exclusion criteria

  • - Cirrhotic patients, those under 18 years of age, additional intraabdominal surgeries during Laparoscopic sleeve gastrectomy and those who had previously undergone obesity surgery (revision surgery) were excluded

Treatment and study plan

Drainage

Other

Using drain after operation

Primary outcomes

  1. Pain Intensity measure

    Time frame: 6 months

    self reported pain intensity morning. item is scored 0-10 ( 0: no pain- 10: pain as bad as can be)

Sponsors and collaborators

Lead sponsor

Inonu University

Other

Registry information

Official study title

Effect of Drain Usage on Patient Comfort on Laparoscopic Sleeve Gastrectomy

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Apr 3, 2020
Registry last updated
Apr 3, 2020

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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