Trials / Terminated
TerminatedNCT00613808
Safety and Efficacy of Gaseous Nitric Oxide on Venous Stasis Leg Ulcers
An Investigation of Topical Application of Gaseous Nitric Oxide on Safety and Efficacy in Venous Stasis Ulcers of the Lower Extremities
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 6 (actual)
- Sponsor
- Nitric BioTherapeutics, Inc · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine whether nitric oxide (NO)gas is effective in the treatment of venous ulcers of the lower leg.
Detailed description
SUbjects were divided into two Groups - one receiving 200ppm NO gas delivered topically to the wound area for 8 hours a day for 6 weeks. The other Group (control arm) received Standard of Care (compression) for 22 weeks.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Nitric Oxide 200ppm Group B | 200 ppm, 8hrs / day for 6 weeks |
Timeline
- Start date
- 2008-02-01
- Primary completion
- 2008-11-01
- Completion
- 2009-05-01
- First posted
- 2008-02-13
- Last updated
- 2012-01-25
Locations
2 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00613808. Inclusion in this directory is not an endorsement.