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NCT03867539 · ClinicalTrials.gov registry record · Phase 4

Exparel and Education to Avoid Opioids After Carpal Tunnel Release

A Phase 4 study of Carpal Tunnel Syndrome, sponsored by Kettering Health Network.

Recruiting
Registry status
Phase 4
Development phase
64
Enrollment target
2
Study locations

NCT03867539: Recruiting Phase 4 study of Carpal Tunnel Syndrome, sponsored by Kettering Health Network.

NCT03867539 is a Phase 4 study of Carpal Tunnel Syndrome that is actively recruiting participants, run by Kettering Health Network. The registered enrollment target is 64 participants, below the 220-participant average among 21 other Carpal Tunnel Syndrome trials with a reported enrollment target (71% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03867539, a Phase 4 study of Carpal Tunnel Syndrome, is actively recruiting participants, sponsored by Kettering Health Network.

RECRUITING
Registry status
Phase 4
Development phase
64 participants
Enrollment target
2
Study locations

Study Summary

This trial seeks to use the long acting local anesthetic Exparel, in conjunction with opioid education, to attempt to avoid any post-operative opioid use following carpal tunnel surgery. This group will be compared with a "standard" group that receives non-liposomal bupivacaine, opioid education, and opioids.

Primary Outcome

The investigators aim to evaluate pain in either arm of the study, followed over a three day course. As several studies have shown pain to be wholly or mostly resolved by post-operative day three. Patients will answer questionnaire to include Visual Analog Scale for pain, and amount of pain medication taken. The Visual Analog Scale for pain ranges from a score of 0 to 10, with 0 being "no pain", 5 being "distressing pain", and 10 being "the worst pain imaginable"

Conditions Studied

Interventions

  • OTHER Differing pain management strategy

Study Locations (2)

Ohio

  • Orthopedic Associates of Southwest Ohio - Dayton
  • Orthopedic Associates of Southwest Ohio - Dayton

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2019-02-15
Est. Completion 2025-03-31
Phase Phase 4
Kettering Health Network

14 total trials

What NCT03867539 shows while recruiting

NCT03867539 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 220-participant average among 21 other Carpal Tunnel Syndrome trials with a reported enrollment target (71% lower).

The record links to 1 condition, with Carpal Tunnel Syndrome appearing as the primary indexed condition, and to 1 intervention - of which Differing pain management strategy is the first listed.

NCT03867539 reports a single indexed study location in Ohio.

Frequently Asked Questions

What is clinical trial NCT03867539 about?

NCT03867539 is a clinical study titled "Exparel and Education to Avoid Opioids After Carpal Tunnel Release". This trial seeks to use the long acting local anesthetic Exparel, in conjunction with opioid education, to attempt to avoid any post-operative opioid use following carpal tunnel surgery. This group will be compared with a "standard" group that receives non-liposomal bupivacaine, opioid education, an...

What is the current status of trial NCT03867539?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 64 participants. The study started on 2019-02-15. Estimated completion is 2025-03-31.

What conditions does trial NCT03867539 study?

This clinical trial studies the following conditions: Carpal Tunnel Syndrome.

What interventions are being tested in trial NCT03867539?

The interventions under investigation include: Differing pain management strategy (OTHER).

Who is sponsoring clinical trial NCT03867539?

This trial is sponsored by Kettering Health Network, which has 14 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03867539 being conducted?

This trial has 2 study locations across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Carpal Tunnel Syndrome

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03867539's enrollment target sits among peer trials

64 15th of 21 higher than 7 of 21 other Carpal Tunnel Syndrome trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Carpal Tunnel Syndrome 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 NCT03867539, the US trial registry maintained by the National Library of Medicine. NCT03867539 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.