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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01247389
Other study ID # 10-183-SDR
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 2011
Est. completion date December 2016

Study information

Verified date August 2018
Source McGill University Health Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Incisional hernia (IH) is a common complication of midline laparotomy. Despite the hope that laparoscopic colon resection would result in fewer incisional hernias, prospective studies demonstrate a similar incidence to open surgery. Observational studies suggest that the rate of incisional hernia after laparoscopic colon resection may be reduced with the use of a transverse compared to a midline extraction incision. However, no randomized trails are available, and a midline extraction incision for hemicolectomy remains the standard current approach. The investigators hypothesize that the use of a lower abdominal transverse muscle splitting incision for specimen extraction in laparoscopic colon surgery will result in fewer incisional hernias compared to a midline periumbilical extraction incision.


Recruitment information / eligibility

Status Completed
Enrollment 165
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- scheduled laparoscopic partial colectomy where an abdominal extraction incision is planned

Exclusion Criteria:

- previous laparotomy

- rectal resection or anastamosis

- planned pfannenstiel extraction incision

- single site surgery

- planned or performed stoma

- BMI >35 kg/m2

- ASA 4-5

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
laparoscopic colectomy
Laparoscopic segmental colectomy with planned abdominal extraction site

Locations

Country Name City State
Canada Montreal General Hospital Montreal Quebec

Sponsors (1)

Lead Sponsor Collaborator
McGill University Health Center

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incisional hernia one year
Secondary surgical site infection one month
Secondary body image one year
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