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NCT05068960 · ClinicalTrials.gov registry record · Phase 4
Postoperative Pain Control in Total Shoulder Arthroplasty
A Phase 4 study, sponsored by Scripps Clinic.
- Completed
- Registry status
- Phase 4
- Development phase
- 100
- Enrollment target
NCT05068960: Completed Phase 4 study, sponsored by Scripps Clinic.
NCT05068960 is a Phase 4 study that has completed, run by Scripps Clinic. The registered enrollment target is 100 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05068960, a Phase 4 study, has completed, sponsored by Scripps Clinic.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 100 participants
- Enrollment target
Study Summary
A double blind, prospective, randomized trial to evaluate postoperative pain, narcotic use, patient satisfaction, and function among shoulder arthroplasty patients receiving interscalene block with and without the addition of liposomal bupivacaine.
Primary Outcome
Number and type of narcotic pain pills consumed during the first postoperative week (also converted into morphine equivalents)
Interventions
- DRUG Bupivacaine
- DRUG Liposomal bupivacaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2021-03-01 |
| Est. Completion | 2025-02-01 |
| Phase | Phase 4 |
What the finished NCT05068960 record still lists
NCT05068960 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower).
The record links to 0 conditions, and to 2 interventions - of which Bupivacaine is the first listed.
NCT05068960 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05068960 about?
NCT05068960 is a clinical study titled "Postoperative Pain Control in Total Shoulder Arthroplasty". A double blind, prospective, randomized trial to evaluate postoperative pain, narcotic use, patient satisfaction, and function among shoulder arthroplasty patients receiving interscalene block with and without the addition of liposomal bupivacaine.
What is the current status of trial NCT05068960?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2021-03-01. Estimated completion is 2025-02-01.
What interventions are being tested in trial NCT05068960?
The interventions under investigation include: Bupivacaine (DRUG), Liposomal bupivacaine (DRUG).
Who is sponsoring clinical trial NCT05068960?
This trial is sponsored by Scripps Clinic, which has 3 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05068960's enrollment target sits among peer trials
100 770th of 2000 higher than 1,148 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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