Status:
COMPLETED
The Intestinal Function in People With Prader-Willi Syndrome
Lead Sponsor:
Aarhus University Hospital
Conditions:
Prader-Willi Syndrome
Constipation
Eligibility:
All Genders
18+ years
Brief Summary
The projects aim is to investigate the intestinal function of patients suffering from Prader-Willi Syndrome. The methods used are ultrasonographic measurement of the rectal diameter and gastrointestin...
Detailed Description
Prader-Willi Syndrome (PWS) is a congenital genetical disease characterized by moderate retardation, food-seeking behavior and a serious risk of developing health threatening overweight, low stature, ...
Eligibility Criteria
Inclusion
- age above 18
- \>14 days since last antibiotic treatment
- \>14 days since last laxative treatment
- PWS confirmed genetically
Exclusion
- previous abdominal surgery (except appendectomy or haemorrhoidectomy
- patient not capable of understanding the information
- treatment with eltroxin or antipsychotic medication
- pregnancy
Key Trial Info
Start Date :
February 1 2011
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
January 1 2012
Estimated Enrollment :
21 Patients enrolled
Trial Details
Trial ID
NCT01523288
Start Date
February 1 2011
End Date
January 1 2012
Last Update
February 1 2012
Active Locations (1)
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1
Centre of Rare Diseases, Pediatric department, Aarhus University Hospital Skejby
Aarhus, Aarhus N, Denmark, 8200