Trials / Terminated
TerminatedNCT00368602
Beta Blocker for Chronic Wound Healing
Beta Adrenergic Receptor Modulation of Burn Wound Healing
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- University of California, Davis · Academic / Other
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the efficacy and safety of treatment of chronic cutaneous ulcers and burn wounds with topical beta adrenergic antagonists (Timoptic®).
Detailed description
The purpose of this study is to learn more about how to heal venous leg ulcers faster and to test the safety of a drug and see what effects it has on a venous leg ulcer. You will: * be interviewed and examined * have a physical exam * have blood and urine tested * have photographs taken of the wound * apply medication to the leg ulcer as directed
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Timoptic | Timoptic to be applied to the target wound daily for up to 12 weeks. |
| OTHER | Placebo | Saline solution with no active ingredients to be applied to the target wound daily for up to 12 weeks. |
Timeline
- Start date
- 2005-06-01
- Primary completion
- 2007-06-01
- Completion
- 2007-06-01
- First posted
- 2006-08-25
- Last updated
- 2015-04-07
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00368602. Inclusion in this directory is not an endorsement.