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NCT01944098 · ClinicalTrials.gov registry record · Phase 3
Intraoperative Lidocaine Infusion for Postoperative Pain Management in Obese Patients
A Phase 3 study, sponsored by University of South Florida.
- Completed
- Registry status
- Phase 3
- Development phase
- 20
- Enrollment target
NCT01944098 is a Phase 3 study that has completed, run by University of South Florida. The registered enrollment target is 20 participants.
The verdict
NCT01944098, a Phase 3 study, has completed, sponsored by University of South Florida.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 20 participants
- Enrollment target
Study Summary
The primary objective is to assess the feasibility and safety of administering continuous intraoperative lidocaine infusions in adult patients undergoing laparoscopic Roux en Y Gastric Bypass (RYGB). The secondary objective is to determine if lidocaine administration versus placebo (dextrose administration) (initiated at the time of anesthesia induction and continued until extubation) will reduce postoperative narcotic requirements.
Interventions
- DRUG Placebo
- DRUG Lidocaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2013-08 |
| Est. Completion | 2014-09 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01944098
The ClinicalTrials.gov registry entry for NCT01944098 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of South Florida, which has 252 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT01944098 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01944098 about?
NCT01944098 is a clinical study titled "Intraoperative Lidocaine Infusion for Postoperative Pain Management in Obese Patients". The primary objective is to assess the feasibility and safety of administering continuous intraoperative lidocaine infusions in adult patients undergoing laparoscopic Roux en Y Gastric Bypass (RYGB). The secondary objective is to determine if lidocaine administration versus placebo (dextrose adminis...
What is the current status of trial NCT01944098?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 20 participants. The study started on 2013-08. Estimated completion is 2014-09.
What interventions are being tested in trial NCT01944098?
The interventions under investigation include: Placebo (DRUG), Lidocaine (DRUG).
Who is sponsoring clinical trial NCT01944098?
This trial is sponsored by University of South Florida, which has 252 total clinical trials registered on ClinicalTrials.gov.
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