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NCT03859635 · ClinicalTrials.gov registry record · Phase 3
Erector Spinae Block Versus Surgeon Infiltration in VATS Procedures
A Phase 3 study of Pain, Postoperative and Acute Pain, sponsored by Indiana University.
- Completed
- Registry status
- Phase 3
- Development phase
- 120
- Enrollment target
- 1
- Study location
NCT03859635 is a Phase 3 study of Pain, Postoperative and Acute Pain that has completed, run by Indiana University. The registered enrollment target is 120 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (56% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03859635, a Phase 3 study of Pain, Postoperative and Acute Pain, has completed, sponsored by Indiana University.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 120 participants
- Enrollment target
- 1
- Study location
Study Summary
The study is comparing the difference between erector spinae block and surgeon infiltration after VATS (Video Assisted Thoracoscopic Surgery). The outcomes measured are pain scores, opioid usage, opioid side effects, and patient satisfaction.We are also also studying the effectiveness of liposomal bupivacaine (EXPAREL) in a block by randomizing patients to both EXPAREL erector spinae block and simple bupivacaine erector spinae block.
Conditions Studied
Interventions
- DRUG Liposomal Bupivacaine
- DRUG Bupivacaine, 0.25%
- DRUG Bupivacaine, 0.5%
Study Locations (1)
Indiana
- Indiana University Hospital - Indianapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2019-02-07 |
| Est. Completion | 2022-11-07 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03859635
The ClinicalTrials.gov registry entry for NCT03859635 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (56% lower). The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 3 interventions - of which Liposomal Bupivacaine is the first listed.
NCT03859635 reports 1 study location spanning 1 distinct geographic area - top geographies include Indiana.
Frequently Asked Questions
What is clinical trial NCT03859635 about?
NCT03859635 is a clinical study titled "Erector Spinae Block Versus Surgeon Infiltration in VATS Procedures". The study is comparing the difference between erector spinae block and surgeon infiltration after VATS (Video Assisted Thoracoscopic Surgery). The outcomes measured are pain scores, opioid usage, opioid side effects, and patient satisfaction.We are also also studying the effectiveness of liposomal b...
What is the current status of trial NCT03859635?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 120 participants. The study started on 2019-02-07. Estimated completion is 2022-11-07.
What conditions does trial NCT03859635 study?
This clinical trial studies the following conditions: Pain, Postoperative, Acute Pain, Thoracic.
What interventions are being tested in trial NCT03859635?
The interventions under investigation include: Liposomal Bupivacaine (DRUG), Bupivacaine, 0.25% (DRUG), Bupivacaine, 0.5% (DRUG).
Who is sponsoring clinical trial NCT03859635?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03859635 being conducted?
This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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