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NCT04084548 · ClinicalTrials.gov registry record · Phase 3
Perioperative Lidocaine and Ketamine in Abdominal Surgery
A Phase 3 study of Postoperative Pain, sponsored by The Cleveland Clinic.
- Active
- Registry status
- Phase 3
- Development phase
- 420
- Enrollment target
- 1
- Study location
NCT04084548 is a Phase 3 study of Postoperative Pain that is active but no longer recruiting, run by The Cleveland Clinic. The registered enrollment target is 420 participants, above the 225-participant average among 63 other Postoperative Pain trials with a reported enrollment target (87% higher). The trial reports 1 study location across 1 state.
The verdict
NCT04084548, a Phase 3 study of Postoperative Pain, is active but no longer recruiting, sponsored by The Cleveland Clinic.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 3
- Development phase
- 420 participants
- Enrollment target
- 1
- Study location
Study Summary
The investigators propose to test the hypothesis that perioperative infusions of lidocaine and/or ketamine reduce opioid consumption and pain scores in adults recovering from elective inpatient abdominal surgery.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Ketamine
- DRUG Lidocaine
- DRUG Lidocaine and ketamine
Study Locations (1)
Florida
- Cleveland Clinic Florida - Weston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 420 participants |
| Start Date | 2019-10-15 |
| Est. Completion | 2025-12 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04084548
The ClinicalTrials.gov registry entry for NCT04084548 describes a study currently listed as active not recruiting, categorized as Phase 3. The registered enrollment target is 420 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 225-participant average among 63 other Postoperative Pain trials with a reported enrollment target (87% higher). The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Postoperative Pain appearing as the primary indexed condition, and to 4 interventions - of which Placebo is the first listed.
NCT04084548 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT04084548 about?
NCT04084548 is a clinical study titled "Perioperative Lidocaine and Ketamine in Abdominal Surgery". The investigators propose to test the hypothesis that perioperative infusions of lidocaine and/or ketamine reduce opioid consumption and pain scores in adults recovering from elective inpatient abdominal surgery.
What is the current status of trial NCT04084548?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 420 participants. The study started on 2019-10-15. Estimated completion is 2025-12.
What conditions does trial NCT04084548 study?
This clinical trial studies the following conditions: Postoperative Pain.
What interventions are being tested in trial NCT04084548?
The interventions under investigation include: Placebo (DRUG), Ketamine (DRUG), Lidocaine (DRUG), Lidocaine and ketamine (DRUG).
Who is sponsoring clinical trial NCT04084548?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04084548 being conducted?
This trial has 1 study location across Florida. 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
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