Clinical Trials Directory

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

TypeNameDescription
DRUGTimopticTimoptic to be applied to the target wound daily for up to 12 weeks.
OTHERPlaceboSaline 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.