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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02469441
Other study ID # 2014-062
Secondary ID
Status Completed
Phase N/A
First received May 29, 2015
Last updated January 19, 2017
Start date August 1, 2014
Est. completion date December 31, 2016

Study information

Verified date January 2017
Source Kantonsspital Baden
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to investigate if postoperative coffee intake decreases the time until first bowel movement in elective colorectal surgery with primary anastomosis.


Description:

Postoperative ileus after colorectal surgery is a frequent problem which significantly prolongs hospital stay and increases perioperative costs. Postoperative therapeutic interventions vary significantly between different hospitals due to missing evidence-based guidelines. Coffee is a safe, cheap and simple agent without significant side effects which can positively influence the bowel function.

The aim of the investigators is to evaluate in an own study if coffee consumption has an influence on the duration of postoperative ileus.

The present trial is designed to evaluate if postoperative coffee intake decreases the time until first bowel movement in colorectal surgery with primary anastomosis. This study would be the second study which evaluates the described questions under randomized conditions.


Recruitment information / eligibility

Status Completed
Enrollment 136
Est. completion date December 31, 2016
Est. primary completion date December 31, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Patients scheduled for elective laparoscopic or open colorectal surgery due to benign or malignant colorectal disease, which need a large bowel resection with primary anastomosis

- Age equal or greater than 18 years

- Patients that are able to give informed consent

- Elective Surgery

- Anastomosis above 6 cm from anal verge

Exclusion Criteria:

- Participation in other studies

- Additional small bowel anastomosis

- Need for extended adhesiolysis

- Need for a stoma (e.g. protective ileostomy)

- Emergency operation with diffuse peritonitis or preexisting ileus

- Preoperative radiation

- Known hypersensitivity or allergy to coffee

- Expected lack of compliance

- Impaired mental state or language problems

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland Kantonsspital Baden BAden

Sponsors (1)

Lead Sponsor Collaborator
Kantonsspital Baden

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to first bowel movement Time to first bowel movement (time from the end of surgery until the first passage of stool recorded by nursing staff) as a marker for the termination of postoperative ileus. Follow-up per patient: 1 month postoperatively
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