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NCT02011464 · ClinicalTrials.gov registry record · Phase 4

Evaluation Exparel Delivered in Knee Replacement

A Phase 4 study, sponsored by Maimonides Medical Center.

Completed
Registry status
Phase 4
Development phase
20
Enrollment target

NCT02011464: Completed Phase 4 study, sponsored by Maimonides Medical Center.

NCT02011464 is a Phase 4 study that has completed, run by Maimonides Medical Center. The registered enrollment target is 20 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02011464, a Phase 4 study, has completed, sponsored by Maimonides Medical Center.

COMPLETED
Registry status
Phase 4
Development phase
20 participants
Enrollment target

Study Summary

Pain control after knee replacement requires analgesia to both the top (anterior) and bottom (posterior) portion of the the knee. Presently we use a nerve block for the anterior portion. The investigators want to to examine if giving Exparel into the posterior portion will give better pain relief. Hypothesis: There is no difference in, the use of analgesics or the length and quality of analgesia and no decrease in the time to be able to accomplish simple to complex knee movements using Exparel infiltration when compared to controls.

Primary Outcome

Subject reported post-surgical pain using the visual analog scale (VAS) during the hospital stay and after discharge. This is a 0-10 point numeric rating scale where 0 is no pain and 10 is the highest level of pain.

Interventions

  • OTHER Saline
  • DRUG Exparel

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2013-12
Est. Completion 2015-09
Phase Phase 4
Maimonides Medical Center

39 total trials

What the finished NCT02011464 record still lists

NCT02011464 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Saline is the first listed.

NCT02011464 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02011464 about?

NCT02011464 is a clinical study titled "Evaluation Exparel Delivered in Knee Replacement". Pain control after knee replacement requires analgesia to both the top (anterior) and bottom (posterior) portion of the the knee. Presently we use a nerve block for the anterior portion. The investigators want to to examine if giving Exparel into the posterior portion will give better pain relief. ...

What is the current status of trial NCT02011464?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2013-12. Estimated completion is 2015-09.

What interventions are being tested in trial NCT02011464?

The interventions under investigation include: Saline (OTHER), Exparel (DRUG).

Who is sponsoring clinical trial NCT02011464?

This trial is sponsored by Maimonides Medical Center, which has 39 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02011464's enrollment target sits among peer trials

20 1753rd of 2000 higher than 167 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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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Source: ClinicalTrials.gov NCT02011464, the US trial registry maintained by the National Library of Medicine. NCT02011464 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.