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NCT00380861 · ClinicalTrials.gov registry record · NA
Does Implant Design Improve Postoperative Flexion?
A NA study, sponsored by DePuy Orthopaedics.
- Completed
- Registry status
- NA
- Development phase
- 93
- Enrollment target
NCT00380861 is a NA study that has completed, run by DePuy Orthopaedics. The registered enrollment target is 93 participants.
The verdict
NCT00380861, a NA study, has completed, sponsored by DePuy Orthopaedics.
- COMPLETED
- Registry status
- NA
- Development phase
- 93 participants
- Enrollment target
Study Summary
This study will evaluate whether design features of one implant design allows more knee bend than the other. Patients will have 1 design in the left knee and 1 design in their right knee. Both knee surgeries will be on the same day.
Interventions
- DEVICE Total knee replacement using the PFC Sigma RPF knee implant.
- DEVICE Total knee replacement using the PFC Sigma RP knee implant
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 93 participants |
| Start Date | 2006-03-01 |
| Est. Completion | 2009-12-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00380861
The ClinicalTrials.gov registry entry for NCT00380861 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 93 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is DePuy Orthopaedics, which has 38 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Total knee replacement using the PFC Sigma RPF knee implant. is the first listed.
NCT00380861 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00380861 about?
NCT00380861 is a clinical study titled "Does Implant Design Improve Postoperative Flexion?". This study will evaluate whether design features of one implant design allows more knee bend than the other. Patients will have 1 design in the left knee and 1 design in their right knee. Both knee surgeries will be on the same day.
What is the current status of trial NCT00380861?
This trial is currently completed. It is a NA study. The enrollment target is 93 participants. The study started on 2006-03-01. Estimated completion is 2009-12-01.
What interventions are being tested in trial NCT00380861?
The interventions under investigation include: Total knee replacement using the PFC Sigma RPF knee implant. (DEVICE), Total knee replacement using the PFC Sigma RP knee implant (DEVICE).
Who is sponsoring clinical trial NCT00380861?
This trial is sponsored by DePuy Orthopaedics, which has 38 total clinical trials registered on ClinicalTrials.gov.
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