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NCT00198042 · ClinicalTrials.gov registry record · NA
Bone Tunnel Widening Following ACL Reconstruction
A NA study, sponsored by Hospital for Special Surgery, New York.
- Completed
- Registry status
- NA
- Development phase
- 18
- Enrollment target
NCT00198042 is a NA study that has completed, run by Hospital for Special Surgery, New York. The registered enrollment target is 18 participants.
The verdict
NCT00198042, a NA study, has completed, sponsored by Hospital for Special Surgery, New York.
- COMPLETED
- Registry status
- NA
- Development phase
- 18 participants
- Enrollment target
Study Summary
Hypothesis 1: There is less tunnel-widening with bone-patella tendon-bone graft compared with the hamstring graft when the same fixation method is used. Tunnel widening is greater with achilles tendon allografts versus autograft bone-patella tendon-bone and hamstring autografts. Hypothesis 2: Tunnel widening occurs in the early post-operative period (\< 8 weeks) when the tendon remodels within the bone tunnels. Hypothesis 3: Low pre-operative bone mineral density is associated with tunnel widening.
Interventions
- PROCEDURE Surgical reconstruction of the ACL
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2004-06 |
| Est. Completion | 2015-12-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00198042
The ClinicalTrials.gov registry entry for NCT00198042 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hospital for Special Surgery, New York, which has 194 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Surgical reconstruction of the ACL is the first listed.
NCT00198042 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00198042 about?
NCT00198042 is a clinical study titled "Bone Tunnel Widening Following ACL Reconstruction". Hypothesis 1: There is less tunnel-widening with bone-patella tendon-bone graft compared with the hamstring graft when the same fixation method is used. Tunnel widening is greater with achilles tendon allografts versus autograft bone-patella tendon-bone and hamstring autografts. Hypothesis 2: Tunne...
What is the current status of trial NCT00198042?
This trial is currently completed. It is a NA study. The enrollment target is 18 participants. The study started on 2004-06. Estimated completion is 2015-12-31.
What interventions are being tested in trial NCT00198042?
The interventions under investigation include: Surgical reconstruction of the ACL (PROCEDURE).
Who is sponsoring clinical trial NCT00198042?
This trial is sponsored by Hospital for Special Surgery, New York, which has 194 total clinical trials registered on ClinicalTrials.gov.
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