Safety Study of Textile Binder for Abdominal Compression
NCT00385892 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11
Last updated 2006-10-11
Summary
This safety study was carried out to investigate to what extent the use of an abdominal binder influences IAP. The study was designed as a comparative cross-over study measuring bladder pressure.
Conditions
- Healthy
Interventions
- DEVICE
-
Abdominal binder
Sponsors & Collaborators
-
Coloplast A/S
lead INDUSTRY
Principal Investigators
-
Lone M Poulsen, Consultant · ITA 303 KAS-Gentofte Niels Andersensvej 65 2900 Hellerup DENMARK
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2005-08-31
- Completion
- 2005-10-31
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