Trials / Completed
CompletedNCT00301496
Randomized Controlled 8-week Crossover Evaluation of Compression Bandage Systems for Venous Leg Ulcers
Randomized Controlled Eight Week Cross-over Clinical Evaluation of the 3M Coban 2-Layer Compression System to Evaluate the Product Performance in Patients With Venous Leg Ulcers
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (planned)
- Sponsor
- Solventum US LLC · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the product performance of a new 2-layer compression bandage for the treatment of venous leg ulcers.
Detailed description
The purpose of this study is to evaluate the product performance of a new 2-layer compression bandage for the treatment of venous leg ulcers. The new bandage is a 2-layer compression system. It will be used over primary dressings to provide the compression that is beneficial to venous leg ulcers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Coban 2 Layer Compression System |
Timeline
- Start date
- 2006-03-01
- Completion
- 2007-04-01
- First posted
- 2006-03-13
- Last updated
- 2024-10-02
Locations
10 sites across 3 countries: United States, Canada, United Kingdom
Source: ClinicalTrials.gov record NCT00301496. Inclusion in this directory is not an endorsement.