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NCT04737980 · ClinicalTrials.gov registry record · Phase 4

Liposomal Bupivacaine Plus Bupivacaine Peripheral Nerve Blockade Versus Ropivacaine Plus Dexamethasone Peripheral Nerve Blockade for Arthroscopic Rotator Cuff Repair

A Phase 4 study of Shoulder Pain and Rotator Cuff Tears, sponsored by Hospital for Special Surgery Florida.

Completed
Registry status
Phase 4
Development phase
92
Enrollment target
1
Study location

NCT04737980 is a Phase 4 study of Shoulder Pain and Rotator Cuff Tears that has completed, run by Hospital for Special Surgery Florida. The registered enrollment target is 92 participants, roughly in line with the 98-participant average among 27 other Shoulder Pain trials with a reported enrollment target. The trial reports 1 study location across 1 state.

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The verdict

NCT04737980, a Phase 4 study of Shoulder Pain and Rotator Cuff Tears, has completed, sponsored by Hospital for Special Surgery Florida.

COMPLETED
Registry status
Phase 4
Development phase
92 participants
Enrollment target
1
Study location

Study Summary

This study is a comparison of analgesia effect from peripheral nerve blockade (PNB) with liposomal bupivacaine combined with bupivacaine compared to PNB with ropivacaine combined with dexamethasone for arthroscopic rotator cuff repair.

Conditions Studied

Shoulder Pain Rotator Cuff Tears

Interventions

  • DRUG Dexamethasone
  • DRUG Ropivacaine 0.5% Injectable Solution
  • DRUG Liposomal bupivacaine
  • DRUG Bupivacaine Hcl 0.5% Inj

Study Locations (1)

Florida

  • HSS Florida - West Palm Beach

Trial Details

FieldValue
Enrollment Target 92 participants
Start Date 2019-07-18
Est. Completion 2020-03-18
Phase Phase 4

Sponsor

Hospital for Special Surgery Florida

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04737980

The ClinicalTrials.gov registry entry for NCT04737980 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 92 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 98-participant average among 27 other Shoulder Pain trials with a reported enrollment target. The listed sponsor is Hospital for Special Surgery Florida, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Shoulder Pain appearing as the primary indexed condition, and to 4 interventions - of which Dexamethasone is the first listed.

NCT04737980 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.

Frequently Asked Questions

What is clinical trial NCT04737980 about?

NCT04737980 is a clinical study titled "Liposomal Bupivacaine Plus Bupivacaine Peripheral Nerve Blockade Versus Ropivacaine Plus Dexamethasone Peripheral Nerve Blockade for Arthroscopic Rotator Cuff Repair". This study is a comparison of analgesia effect from peripheral nerve blockade (PNB) with liposomal bupivacaine combined with bupivacaine compared to PNB with ropivacaine combined with dexamethasone for arthroscopic rotator cuff repair.

What is the current status of trial NCT04737980?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 92 participants. The study started on 2019-07-18. Estimated completion is 2020-03-18.

What conditions does trial NCT04737980 study?

This clinical trial studies the following conditions: Shoulder Pain, Rotator Cuff Tears.

What interventions are being tested in trial NCT04737980?

The interventions under investigation include: Dexamethasone (DRUG), Ropivacaine 0.5% Injectable Solution (DRUG), Liposomal bupivacaine (DRUG), Bupivacaine Hcl 0.5% Inj (DRUG).

Who is sponsoring clinical trial NCT04737980?

This trial is sponsored by Hospital for Special Surgery Florida, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04737980 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.