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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03826251
Other study ID # UH Angers 2018/75
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2014
Est. completion date June 1, 2018

Study information

Verified date January 2019
Source University Hospital, Angers
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Postoperative management after small bowel obstruction (SBO) surgery is not consensual and better knowledge of risk factors for postoperative morbidity could help to add evidence of the feasibility of enhanced recovery programs (ERPs).

In elective surgery, ERPs have shown a significant benefit for the patient but this is not performed routinely in emergency surgery due to the difficulty to avoid postoperative nasogastric tube.

The aim was to identify risk factors for postoperative morbidity and for nasogastric tube (NGT) replacement after SBO surgery.


Recruitment information / eligibility

Status Completed
Enrollment 190
Est. completion date June 1, 2018
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria:

- Surgical management of Small bowel obstruction due to adhesions

Exclusion Criteria:

- obstruction not caused by single band adhesion

- matted adhesions, or if they were less than 18 years old

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Nasogastric tube removal
Nasogastric tube was removed immediately after surgery

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Angers

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative morbidity morbidity classified according to Dindo Clavien classification within 30 days
Secondary Nasogastric tube replacement nasogastric tube replacement after removal within 30 days