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NCT03253198 · ClinicalTrials.gov registry record · NA
Prospective RCT Comparing Perioperative Pain
A NA study of Arthroplasty Shoulder, sponsored by Rothman Institute Orthopaedics.
- Completed
- Registry status
- NA
- Development phase
- 156
- Enrollment target
- 1
- Study location
NCT03253198 is a NA study of Arthroplasty Shoulder that has completed, run by Rothman Institute Orthopaedics. The registered enrollment target is 156 participants. The trial reports 1 study location across 1 state.
The verdict
NCT03253198, a NA study of Arthroplasty Shoulder, has completed, sponsored by Rothman Institute Orthopaedics.
- COMPLETED
- Registry status
- NA
- Development phase
- 156 participants
- Enrollment target
- 1
- Study location
Study Summary
This study is a non-blinded randomized controlled trial comparing the use of a preoperative "mini" block plus postoperative local infiltration of Exparel (liposomal form of bupivacaine) versus a partial single shot nerve block in subjects undergoing primary reverse or total shoulder arthroplasty to see which is more effective in controlling surgery related pain. To do so, we will utilize the Visual Analog Scale (VAS) to measure pain intensity. Opioid consumption will be recorded on a Pain Monitoring Sheet.
Conditions Studied
Interventions
- DRUG Saline
- DRUG Bupivacaine liposome
Study Locations (1)
Pennsylvania
- Rothman Institute - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 156 participants |
| Start Date | 2016-08 |
| Est. Completion | 2017-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03253198
The ClinicalTrials.gov registry entry for NCT03253198 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 156 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rothman Institute Orthopaedics, which has 23 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Arthroplasty Shoulder appearing as the primary indexed condition, and to 2 interventions - of which Saline is the first listed.
NCT03253198 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT03253198 about?
NCT03253198 is a clinical study titled "Prospective RCT Comparing Perioperative Pain". This study is a non-blinded randomized controlled trial comparing the use of a preoperative "mini" block plus postoperative local infiltration of Exparel (liposomal form of bupivacaine) versus a partial single shot nerve block in subjects undergoing primary reverse or total shoulder arthroplasty to ...
What is the current status of trial NCT03253198?
This trial is currently completed. It is a NA study. The enrollment target is 156 participants. The study started on 2016-08. Estimated completion is 2017-07.
What conditions does trial NCT03253198 study?
This clinical trial studies the following conditions: Arthroplasty Shoulder.
What interventions are being tested in trial NCT03253198?
The interventions under investigation include: Saline (DRUG), Bupivacaine liposome (DRUG).
Who is sponsoring clinical trial NCT03253198?
This trial is sponsored by Rothman Institute Orthopaedics, which has 23 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03253198 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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