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NCT00695578 · ClinicalTrials.gov registry record · Phase 4
Clinical Trial to Evaluate Biafine Cream Versus Standard Care in Subjects With Actinic Keratosis Post Cryotherapy
A Phase 4 study of Actinic Keratosis, sponsored by Wake Forest University.
- Completed
- Registry status
- Phase 4
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT00695578 is a Phase 4 study of Actinic Keratosis that has completed, run by Wake Forest University. The registered enrollment target is 20 participants, below the 188-participant average among 16 other Actinic Keratosis trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00695578, a Phase 4 study of Actinic Keratosis, has completed, sponsored by Wake Forest University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this research study is to evaluate the use of Biafine Cream on wounds created by removal of actinic keratosis using cryotherapy in a clinical setting.
Conditions Studied
Interventions
- DRUG Biafine
- DRUG Polysporin
Study Locations (1)
North Carolina
- Wake Forest University Health Sciences Dermatology - Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2006-10 |
| Est. Completion | 2008-02 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00695578
The ClinicalTrials.gov registry entry for NCT00695578 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 188-participant average among 16 other Actinic Keratosis trials with a reported enrollment target (89% lower). The listed sponsor is Wake Forest University, which has 100 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Actinic Keratosis appearing as the primary indexed condition, and to 2 interventions - of which Biafine is the first listed.
NCT00695578 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.
Frequently Asked Questions
What is clinical trial NCT00695578 about?
NCT00695578 is a clinical study titled "Clinical Trial to Evaluate Biafine Cream Versus Standard Care in Subjects With Actinic Keratosis Post Cryotherapy". The purpose of this research study is to evaluate the use of Biafine Cream on wounds created by removal of actinic keratosis using cryotherapy in a clinical setting.
What is the current status of trial NCT00695578?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2006-10. Estimated completion is 2008-02.
What conditions does trial NCT00695578 study?
This clinical trial studies the following conditions: Actinic Keratosis.
What interventions are being tested in trial NCT00695578?
The interventions under investigation include: Biafine (DRUG), Polysporin (DRUG).
Who is sponsoring clinical trial NCT00695578?
This trial is sponsored by Wake Forest University, which has 100 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00695578 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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