Trials / Completed
CompletedNCT01910896
Effectiveness and Safety Study of Overnight Intensive Patch in Scars
A Prospective, Intra-individual Randomized, Observer-blind, Controlled Investigation to Investigate the Effectiveness and Safety of Overnight Intensive Patch (OIP) Over 12 to 24 Weeks in Post Dermatological Surgery Scars
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 125 (actual)
- Sponsor
- Merz Pharmaceuticals GmbH · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To investigate the effectiveness of an Overnight Intensive Patch (OIP) on improvement of post dermatological surgery scars and its safety over 12 to 24 weeks.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Overnight Intensive Patch | Eligible subjects will have their two scars randomized for OIP application/no treatment. OIP for overnight application (at least 6 hours) for 12 to 24 weeks. |
Timeline
- Start date
- 2013-10-01
- Primary completion
- 2015-05-01
- Completion
- 2015-07-01
- First posted
- 2013-07-30
- Last updated
- 2015-09-09
Locations
9 sites across 1 country: Germany
Source: ClinicalTrials.gov record NCT01910896. Inclusion in this directory is not an endorsement.