Trials / Completed
CompletedNCT00900029
Safety Follow-Up to HP 802-247-09-015
A Twenty-Four Week Non-Interventional Safety Follow-Up to HP 802-247-09-015
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 206 (actual)
- Sponsor
- Healthpoint · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a 24-week observational follow safety study for Study 802-247-09-015.
Detailed description
The objective of this study is to examine the durability of previous target wound closures, identify new test article-related adverse events, record new target wound closures, and examine ongoing adverse events not resolved in subjects who participated in HP 802-247-09-015.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | No HP802 Treatment | |
| OTHER | No HP802 Vehicle Treatment |
Timeline
- Start date
- 2009-06-01
- Primary completion
- 2011-10-01
- Completion
- 2012-01-01
- First posted
- 2009-05-12
- Last updated
- 2017-08-02
- Results posted
- 2016-09-29
Locations
30 sites across 2 countries: United States, Canada
Source: ClinicalTrials.gov record NCT00900029. Inclusion in this directory is not an endorsement.