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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01326052
Other study ID # DS-004
Secondary ID
Status Completed
Phase Phase 3
First received March 25, 2011
Last updated June 12, 2012
Start date January 2004
Est. completion date December 2011

Study information

Verified date June 2012
Source University of Roma La Sapienza
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Interventional

Clinical Trial Summary

The aim of the study is to evaluate the anorectal function after hemicolectomy if we preserve or not the Inferior Mesenteric Artery (IMA). This study wants to demonstrate that IMA preservation could improve patient's quality of life reducing incontinence and/or constipation rate.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date December 2011
Est. primary completion date January 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Age from 18 to 80 years

- BMI<35

- Presence of symptomatic diverticular disease

- ASA I-III

Exclusion Criteria:

- age > 80 years

- BMI>35

- ASA IV

- Hinchey III-IV

- Past performed procedure that could be modify the nervous pattern (i.e. colorectal surgery, left nephrectomy, hysteroannessectomy)

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Defecatory Disorders After Left Colonic or Rectal Resection
  • Diverticulum

Intervention

Procedure:
Inferior Mesenteric Artery Preservation
Performing left hemicolectomy the IMA was preserved ligating close to the colonic wall the sigmoids arteries.
Inferior Mesenteric Artery Ligation
Performing left hemicolectomy the IMA is ligated and sectioned after the origin of left colic artery

Locations

Country Name City State
Italy Azienda Ospedaliera Sant'Andrea Rome

Sponsors (1)

Lead Sponsor Collaborator
University of Roma La Sapienza

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from preoperative time in anorectal function We evaluate the presence of modification in anorectal function respect to the preoperative time. This is assessed with specific questionnnaires and anorectal manometry 6 and 12 months No
Secondary Constipation We evaluate with a questionnaire (Constipation scoring system) the presence of postoperative constipation 6 and 12 months No
Secondary Incontinence We evaluate with a questionnaire (Continence scale), anorectal manometry and eventually with endoanal ultrasonography the precence of incontinence 6 and 12 months No
Secondary Quality of life We evaluate with SF-36 questionnaire the postoperative quality of life 6 and 12 months No
Secondary Postoperative complication We evaluate the presence of postoperative complication such as anastomotic leakage, anastomotic stricture, pneumonia etc. 1 month Yes