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NCT01602484 · ClinicalTrials.gov registry record · NA
Application Time of Plaster-of-Paris Splint Packs Compared to Bulk Supplies Following Standard Orthopaedic Procedure
A NA study, sponsored by Brigham and Women's Hospital.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
NCT01602484: Completed NA study, sponsored by Brigham and Women's Hospital.
NCT01602484 is a NA study that has completed, run by Brigham and Women's Hospital. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01602484, a NA study, has completed, sponsored by Brigham and Women's Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
Study Summary
The investigators wish to perform a randomized controlled study to determine how much time and money is saved by orthopedic foot and ankle surgeons through the use of prepared splint packs compared to bulk supplies.
Primary Outcome
Time it takes to apply post-op splint
Interventions
- DEVICE Pre-prepared Splint Pack composed by Medline
- DEVICE Bulk splint supplies
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2011-10 |
| Est. Completion | 2012-07 |
| Phase | NA |
What the finished NCT01602484 record still lists
NCT01602484 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 2 interventions - of which Pre-prepared Splint Pack composed by Medline is the first listed.
NCT01602484 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01602484 about?
NCT01602484 is a clinical study titled "Application Time of Plaster-of-Paris Splint Packs Compared to Bulk Supplies Following Standard Orthopaedic Procedure". The investigators wish to perform a randomized controlled study to determine how much time and money is saved by orthopedic foot and ankle surgeons through the use of prepared splint packs compared to bulk supplies.
What is the current status of trial NCT01602484?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2011-10. Estimated completion is 2012-07.
What interventions are being tested in trial NCT01602484?
The interventions under investigation include: Pre-prepared Splint Pack composed by Medline (DEVICE), Bulk splint supplies (DEVICE).
Who is sponsoring clinical trial NCT01602484?
This trial is sponsored by Brigham and Women's Hospital, which has 937 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01602484's enrollment target sits among peer trials
50 1279th of 2000 higher than 622 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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