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NCT03151434 · ClinicalTrials.gov registry record · Phase 3
Comparison of Three Different Pain Blocks for Subjects Undergoing VATS (Video Assisted Thoracoscopic Surgery) Procedure.
A Phase 3 study of Pain, Postoperative and Pain, Acute, sponsored by Indiana University.
- Completed
- Registry status
- Phase 3
- Development phase
- 147
- Enrollment target
- 1
- Study location
NCT03151434 is a Phase 3 study of Pain, Postoperative and Pain, Acute that has completed, run by Indiana University. The registered enrollment target is 147 participants, below the 271-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (46% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03151434, a Phase 3 study of Pain, Postoperative and Pain, Acute, has completed, sponsored by Indiana University.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 147 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare three different pain control methods on subjects who are scheduled to undergo VATS (video-assisted thoracoscopic surgery) procedures. The study will compare their pain scores, narcotic needs, patient satisfaction scores, and narcotic side effects.
Conditions Studied
Interventions
- DRUG US Guided Single Shot Paravertebral Block (0.2% ropivicaine infusion)
- DRUG US Guided Paravertebral Catheter (0.2% ropivicaine bolus)
- DRUG Thoracic Epidural (0.125% bupivicaine/hydromorphone)
Study Locations (1)
Indiana
- Indiana University Hospital - Indianapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 147 participants |
| Start Date | 2017-02-07 |
| Est. Completion | 2018-07-30 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03151434
The ClinicalTrials.gov registry entry for NCT03151434 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 147 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 271-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (46% 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 US Guided Single Shot Paravertebral Block (0.2% ropivicaine infusion) is the first listed.
NCT03151434 reports 1 study location spanning 1 distinct geographic area - top geographies include Indiana.
Frequently Asked Questions
What is clinical trial NCT03151434 about?
NCT03151434 is a clinical study titled "Comparison of Three Different Pain Blocks for Subjects Undergoing VATS (Video Assisted Thoracoscopic Surgery) Procedure.". The purpose of this study is to compare three different pain control methods on subjects who are scheduled to undergo VATS (video-assisted thoracoscopic surgery) procedures. The study will compare their pain scores, narcotic needs, patient satisfaction scores, and narcotic side effects.
What is the current status of trial NCT03151434?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 147 participants. The study started on 2017-02-07. Estimated completion is 2018-07-30.
What conditions does trial NCT03151434 study?
This clinical trial studies the following conditions: Pain, Postoperative, Pain, Acute, Video Assisted Thoracoscopic Surgery.
What interventions are being tested in trial NCT03151434?
The interventions under investigation include: US Guided Single Shot Paravertebral Block (0.2% ropivicaine infusion) (DRUG), US Guided Paravertebral Catheter (0.2% ropivicaine bolus) (DRUG), Thoracic Epidural (0.125% bupivicaine/hydromorphone) (DRUG).
Who is sponsoring clinical trial NCT03151434?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03151434 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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Read our methodology - how this data is sourced, computed, and verified.
Related
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.