drugset / Trial / NCT07632144
Ondansetron Versus Lidocaine for Preventing Pain on Propofol Injection.
RandomizedParallel-groupTriple-blindPrevention
Summary
This is a prospective, single-center, randomized, double-blind controlled trial involving patients scheduled for elective surgery requiring general anesthesia with propofol induction. Participants are randomly assigned to one of three groups: the ondansetron group (8 mg IV), the lidocaine group (40 mg IV), or the control group (0.9% normal saline placebo). Study medications are administered intravenously over 5 minutes, ending 1 minute before anesthetic induction. the goal: To assess the efficacy of intravenous ondansetron versus lidocaine and placebo in reducing the incidence and intensity of pain associated with propofol injection in patients undergoing general anesthesia.
Timeline
- Start
- 2026-06-08
- Primary completion
- 2026-07-30
- Completion
- 2026-08-15
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Lidocaine | Other / unclassified | 40 mg | Intravenous |
| Subject | Ondansetron | Other / unclassified | 8 mg | Intravenous |
Indications
No indication recorded.