Comparison Study of 3 Ostomy Products
NCT01691729 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 26
Last updated 2022-12-07
Summary
To purpose of the study is to evaluate and compare the efficacy of three ostomy accessory products.
Conditions
- Ostomy
Interventions
- DEVICE
-
Ostomy accessory
Wearing each of the devices for 10 days each
Sponsors & Collaborators
-
ConvaTec Inc.
lead INDUSTRY
Principal Investigators
-
Kim Peters · ConvaTec Inc.
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2012-09-30
- Primary Completion
- 2012-11-30
- Completion
- 2012-11-30
Countries
- United States
Study Locations
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