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NCT02061774 · ClinicalTrials.gov registry record · Phase 4
Postoperative Opioid Use and Pain Scores in Patients Undergoing Transforaminal Lumbar Interbody Fusion
A Phase 4 study, sponsored by Texas Tech University Health Sciences Center.
- Terminated
- Registry status
- Phase 4
- Development phase
- 21
- Enrollment target
NCT02061774 is a Phase 4 study that was terminated before completion, run by Texas Tech University Health Sciences Center. The registered enrollment target is 21 participants.
The verdict
NCT02061774, a Phase 4 study, was terminated before completion, sponsored by Texas Tech University Health Sciences Center.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 21 participants
- Enrollment target
Study Summary
The purpose of this project is to study the effects of preoperative followed by scheduled intravenous acetaminophen on pain control for 24 hours postoperatively after minimally invasive 1 or 2 level transforaminal lumbar interbody fusion.
Interventions
- DRUG Acetaminophen
- DRUG Placebo comparator
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 21 participants |
| Start Date | 2013-10 |
| Est. Completion | 2018-01-11 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02061774
The ClinicalTrials.gov registry entry for NCT02061774 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Texas Tech University Health Sciences Center, which has 76 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Acetaminophen is the first listed.
NCT02061774 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02061774 about?
NCT02061774 is a clinical study titled "Postoperative Opioid Use and Pain Scores in Patients Undergoing Transforaminal Lumbar Interbody Fusion". The purpose of this project is to study the effects of preoperative followed by scheduled intravenous acetaminophen on pain control for 24 hours postoperatively after minimally invasive 1 or 2 level transforaminal lumbar interbody fusion.
What is the current status of trial NCT02061774?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 21 participants. The study started on 2013-10. Estimated completion is 2018-01-11.
What interventions are being tested in trial NCT02061774?
The interventions under investigation include: Acetaminophen (DRUG), Placebo comparator (DRUG).
Who is sponsoring clinical trial NCT02061774?
This trial is sponsored by Texas Tech University Health Sciences Center, which has 76 total clinical trials registered on ClinicalTrials.gov.
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