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NCT00763386 · ClinicalTrials.gov registry record · NA
A Study to Compare the NexGen LPS and LPS-Flex Knee Implants
A NA study, sponsored by Zimmer Biomet.
- Completed
- Registry status
- NA
- Development phase
- 331
- Enrollment target
NCT00763386 is a NA study that has completed, run by Zimmer Biomet. The registered enrollment target is 331 participants.
The verdict
NCT00763386, a NA study, has completed, sponsored by Zimmer Biomet.
- COMPLETED
- Registry status
- NA
- Development phase
- 331 participants
- Enrollment target
Study Summary
The purpose of this study is to test for significant differences in functional outcomes obtained by using a NexGen LPS versus a NexGen LPS-Flex knee implant. Specifically, it is predicted that an increase in postoperative range of motion will be experienced by patients treated with the NexGen LPS-Flex knee implant.
Interventions
- DEVICE NexGen LPS-Flex Fixed Bearing Knee
- DEVICE NexGen Legacy Posterior Stabilized Knee
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 331 participants |
| Start Date | 2001-06 |
| Est. Completion | 2010-03 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00763386
The ClinicalTrials.gov registry entry for NCT00763386 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 331 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Zimmer Biomet, which has 115 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which NexGen LPS-Flex Fixed Bearing Knee is the first listed.
NCT00763386 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00763386 about?
NCT00763386 is a clinical study titled "A Study to Compare the NexGen LPS and LPS-Flex Knee Implants". The purpose of this study is to test for significant differences in functional outcomes obtained by using a NexGen LPS versus a NexGen LPS-Flex knee implant. Specifically, it is predicted that an increase in postoperative range of motion will be experienced by patients treated with the NexGen LPS-Fl...
What is the current status of trial NCT00763386?
This trial is currently completed. It is a NA study. The enrollment target is 331 participants. The study started on 2001-06. Estimated completion is 2010-03.
What interventions are being tested in trial NCT00763386?
The interventions under investigation include: NexGen LPS-Flex Fixed Bearing Knee (DEVICE), NexGen Legacy Posterior Stabilized Knee (DEVICE).
Who is sponsoring clinical trial NCT00763386?
This trial is sponsored by Zimmer Biomet, which has 115 total clinical trials registered on ClinicalTrials.gov.
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