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NCT00971048 · ClinicalTrials.gov registry record · NA
Evaluation of the Effects of HP828-101 Versus Standard of Care in the Management of Partial or Full Thickness Wounds
A NA study, sponsored by Healthpoint.
- Completed
- Registry status
- NA
- Development phase
- 88
- Enrollment target
NCT00971048: Completed NA study, sponsored by Healthpoint.
NCT00971048 is a NA study that has completed, run by Healthpoint. The registered enrollment target is 88 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00971048, a NA study, has completed, sponsored by Healthpoint.
- COMPLETED
- Registry status
- NA
- Development phase
- 88 participants
- Enrollment target
Study Summary
To compare HP828-101 to standard of care for the management of partial or full thickness wounds
Primary Outcome
Modified Bates-Jensen Wound Assessment (BWAT-m) Scores for those characteristics measured (wound size, depth, edges, undermining, necrotic tissue type and amount, exudate type and amount, periwound color and edema, granulation tissue, and epithelialization) were each graded on a 5-point scale, with 1 being the best and 5 being the worst.
Interventions
- DEVICE HP828-101
- DEVICE Hydrogel/Hydrocolloid
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 88 participants |
| Start Date | 2009-09 |
| Est. Completion | 2011-01 |
| Phase | NA |
What the finished NCT00971048 record still lists
NCT00971048 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 88 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).
The record links to 0 conditions, and to 2 interventions - of which HP828-101 is the first listed.
NCT00971048 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00971048 about?
NCT00971048 is a clinical study titled "Evaluation of the Effects of HP828-101 Versus Standard of Care in the Management of Partial or Full Thickness Wounds". To compare HP828-101 to standard of care for the management of partial or full thickness wounds
What is the current status of trial NCT00971048?
This trial is currently completed. It is a NA study. The enrollment target is 88 participants. The study started on 2009-09. Estimated completion is 2011-01.
What interventions are being tested in trial NCT00971048?
The interventions under investigation include: HP828-101 (DEVICE), Hydrogel/Hydrocolloid (DEVICE).
Who is sponsoring clinical trial NCT00971048?
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 NCT00971048's enrollment target sits among peer trials
88 972nd of 2000 higher than 1,027 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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