Congenital malrotation in adults

Not Applicable

Completed

• Conditions: Congenital intestinal malrotation; Digestive System

• Registration Number: ISRCTN63794639
• Lead Sponsor: Karolinska Institutet

Brief Summary

2016 results in https://www.ncbi.nlm.nih.gov/pubmed/27026938 (added 02/04/2020)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-02-25
• Study Completion: 2018-12-31
• Last Update Posted: 27 April 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 39

Inclusion Criteria

1. Aged 16 years or over
2. Abdominal pain
3. Malrotation on CT scan

Exclusion Criteria

1. Not understanding oral or written information
2. Under 15 years of age

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Symptom resolution following surgery is determined using semi-structured telephone interviews with a research nurse, during 2012-2013 (1 to 12 years after surgery).

Secondary Outcome Measures

Name	Time	Method
Degree of malrotation is determined using CT scanning at baseline.