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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: Completed NA study, sponsored by Zimmer Biomet.
NCT00763386 is a NA study that has completed, run by Zimmer Biomet. The registered enrollment target is 331 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (76% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Postoperative ROM was calculated by taking the measurement of patient flexion minus the measurement of patients' extension.
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 |
What the finished NCT00763386 record still lists
NCT00763386 is an interventional study that assigns participants to a tested intervention. The registered 331 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (76% lower).
The record links to 0 conditions, and to 2 interventions - of which NexGen LPS-Flex Fixed Bearing Knee is the first listed.
NCT00763386 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00763386's enrollment target sits among peer trials
331 307th of 2000 higher than 1,694 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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