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NCT03499769 Clinical Trial

Comparison of NOSE and Conventional Methods in Laparoscopic Total Colon Surgery

Surgical Incision Clinical Trial

Official title:
Comparison of NOSE and Conventional Methods in Laparoscopic Total Colon Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03499769
Other study ID # 2018/3-3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2013
Est. completion date December 28, 2017

Study information
Verified date February 2018
Source Inonu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Laparoscopic total colectomy (LTC) is an accepted surgical procedure for several colonic pathologies. Additionally, specimen extraction through the natural orifices is an emerging method when combined with the totally laparoscopic procedures. Our observations on natural orifice surgery was promising . In our daily surgical practice, investigators prefer the intracorporeal anastomosis and this study was conducted to compare the specimen extraction sites after LTC. Here investigators aimed to compare the results of conventional and natural orifice specimen extractions (NOSE) after totally LTCs.

Description:

compare the patient-selected NOSE method and conventional method in laparoscopic total colon surgery

Recruitment information / eligibility
Status Completed
Enrollment 26
Est. completion date December 28, 2017
Est. primary completion date December 25, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- laparoscopic total colectomy patients

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• natural orifice
laparoscopic total colon surgery and patients who are removed from the natural orifice and conventional will gather

Locations
Country Name City State
Turkey Inonu University Malatya

Sponsors (1)
Lead Sponsor Collaborator
Inonu University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Visual Analog Score Visual Analog Score for pain (1-10 score) 240 days
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