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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03231423
Other study ID # 2016/181
Secondary ID
Status Completed
Phase N/A
First received July 12, 2017
Last updated July 26, 2017
Start date December 9, 2016
Est. completion date June 22, 2017

Study information

Verified date July 2017
Source Inonu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Description:

Question the necessity of routine use of drain in RYGB surgeon


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date June 22, 2017
Est. primary completion date June 22, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Drainage
Using drain after operation

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Inonu University

Outcome

Type Measure Description Time frame Safety issue
Primary 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) 8 months
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