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NCT01253135 · ClinicalTrials.gov registry record · Phase 1
Study to Determine if Fibrin Affects the Ability of a Wound to Heal
A Phase 1 study, sponsored by Healthpoint.
- Completed
- Registry status
- Phase 1
- Development phase
- 40
- Enrollment target
NCT01253135: Completed Phase 1 study, sponsored by Healthpoint.
NCT01253135 is a Phase 1 study that has completed, run by Healthpoint. The registered enrollment target is 40 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01253135, a Phase 1 study, has completed, sponsored by Healthpoint.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 40 participants
- Enrollment target
Study Summary
The objective of this study is to evaluate the potential inhibitory effects of HP802-247 Vehicle on wound closure (healing), by comparing mean days to closure of superficial (partial-thickness) thermal wounds against similar wounds treated with white petrolatum.
Primary Outcome
The target wounds were evaluated wound status (open/closed).
Interventions
- OTHER White Petrolatum
- BIOLOGICAL Fibrin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2011-01 |
| Est. Completion | 2011-11 |
| Phase | Phase 1 |
What the finished NCT01253135 record still lists
NCT01253135 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).
The record links to 0 conditions, and to 2 interventions - of which White Petrolatum is the first listed.
NCT01253135 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01253135 about?
NCT01253135 is a clinical study titled "Study to Determine if Fibrin Affects the Ability of a Wound to Heal". The objective of this study is to evaluate the potential inhibitory effects of HP802-247 Vehicle on wound closure (healing), by comparing mean days to closure of superficial (partial-thickness) thermal wounds against similar wounds treated with white petrolatum.
What is the current status of trial NCT01253135?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2011-01. Estimated completion is 2011-11.
What interventions are being tested in trial NCT01253135?
The interventions under investigation include: White Petrolatum (OTHER), Fibrin (BIOLOGICAL).
Who is sponsoring clinical trial NCT01253135?
This trial is sponsored by Healthpoint, which has 25 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01253135's enrollment target sits among peer trials
40 1130th of 2000 higher than 810 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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