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NCT00689962 · ClinicalTrials.gov registry record · Phase 4
A Comparison of Steel and Bioabsorbable Screw Fixation of Lisfranc Foot Injuries
A Phase 4 study, sponsored by Rothman Institute Orthopaedics.
- Completed
- Registry status
- Phase 4
- Development phase
- 50
- Enrollment target
NCT00689962 is a Phase 4 study that has completed, run by Rothman Institute Orthopaedics. The registered enrollment target is 50 participants.
The verdict
NCT00689962, a Phase 4 study, has completed, sponsored by Rothman Institute Orthopaedics.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 50 participants
- Enrollment target
Study Summary
I hypothesize that absorbable screw fixation of the foot's Lisfranc ligaments does not yield significant differences in postoperative foot stability, ligament function, and symptoms when compared to steel screw fixation. In addition, absorbable screw fixation of the Lisfranc ligaments offers the advantage that a second surgical procedure to remove the screw is not necessary.
Interventions
- DEVICE Linvatec 4.5 mm Smart Screw
- DEVICE Synthes 4.0 mm steel screw
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2008-07 |
| Est. Completion | 2016-07 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00689962
The ClinicalTrials.gov registry entry for NCT00689962 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rothman Institute Orthopaedics, which has 23 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Linvatec 4.5 mm Smart Screw is the first listed.
NCT00689962 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00689962 about?
NCT00689962 is a clinical study titled "A Comparison of Steel and Bioabsorbable Screw Fixation of Lisfranc Foot Injuries". I hypothesize that absorbable screw fixation of the foot's Lisfranc ligaments does not yield significant differences in postoperative foot stability, ligament function, and symptoms when compared to steel screw fixation. In addition, absorbable screw fixation of the Lisfranc ligaments offers the adv...
What is the current status of trial NCT00689962?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2008-07. Estimated completion is 2016-07.
What interventions are being tested in trial NCT00689962?
The interventions under investigation include: Linvatec 4.5 mm Smart Screw (DEVICE), Synthes 4.0 mm steel screw (DEVICE).
Who is sponsoring clinical trial NCT00689962?
This trial is sponsored by Rothman Institute Orthopaedics, which has 23 total clinical trials registered on ClinicalTrials.gov.
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