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Effect of Drainage on Laparoscopic Gastric Bypass Surgery

Primary Purpose

Obesity, Morbid

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Drainage
Sponsored by
Inonu University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity, Morbid focused on measuring Obesity, VAS, Pain, Laparoscopy, Bypass

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Morbid obese patients

Exclusion Criteria:

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

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    DRAIN PLACEMENT

    DRAIN NOT PLACED

    Arm Description

    Effects of drainage

    Effects of not using drain

    Outcomes

    Primary Outcome Measures

    3-Item Pain Intensity measyre (P3)
    self reported pain intensity morning, second day and third day. Each item is scored 0-10 ( 0: no pain- 10: pain as bad as can be)

    Secondary Outcome Measures

    Full Information

    First Posted
    July 12, 2017
    Last Updated
    July 26, 2017
    Sponsor
    Inonu University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03231423
    Brief Title
    Effect of Drainage on Laparoscopic Gastric Bypass Surgery
    Official Title
    Effect of Drain Usage on Patient Comfort on Laparoscopic Gastric Bypass Surgery
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    December 9, 2016 (Actual)
    Primary Completion Date
    June 22, 2017 (Actual)
    Study Completion Date
    June 22, 2017 (Actual)

    3. Sponsor/Collaborators

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

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Introduction RYGB 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.
    Detailed Description
    Question the necessity of routine use of drain in RYGB surgeon

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Obesity, Morbid
    Keywords
    Obesity, VAS, Pain, Laparoscopy, Bypass

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    66 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    DRAIN PLACEMENT
    Arm Type
    Experimental
    Arm Description
    Effects of drainage
    Arm Title
    DRAIN NOT PLACED
    Arm Type
    No Intervention
    Arm Description
    Effects of not using drain
    Intervention Type
    Other
    Intervention Name(s)
    Drainage
    Intervention Description
    Using drain after operation
    Primary Outcome Measure Information:
    Title
    3-Item Pain Intensity measyre (P3)
    Description
    self reported pain intensity morning, second day and third day. Each item is scored 0-10 ( 0: no pain- 10: pain as bad as can be)
    Time Frame
    8 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Morbid obese patients Exclusion Criteria: Cirrhotic patients, those under 18 years of age, additional intraabdominal surgeries during LRYGBP and those who had previously undergone obesity surgery (revision surgery) were excluded

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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