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Effects of total intravenous anesthesia with propofol versus sevoflurane anesthesia on postoperative nausea and vomiting in patients undergoing microvascular decompression surgery: A randomized controlled trial

Effects of total intravenous anesthesia with propofol versus sevoflurane anesthesia on postoperative nausea and vomiting in patients undergoing microvascular decompression surgery: A randomized controlled trial

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250812005
Enrollment
58
Registered
2025-08-12
Start date
2025-08-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

preventing PONV in patients who underwent MVD surgery Microvascular decompression surgery (MDV) Postoperative nausea and vomiting (PONV) Propofol infusion

Interventions

induction by Target Controlled Infusions ( TCI) of propofol infusion, Monitor Bispectral index, keep value between 40- 60 maintenance anesthesia with Target Controlled Infusions (TCI) of propofol inf
TIVA with Propofol,Sevoflurane

Sponsors

Khon Kaen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-65 years old 2. ASA physical status I III

Exclusion criteria

Exclusion criteria: 1. refuse to participate 2. History of PONV, motion sickness 3. Known allergies to study drugs: propofol, dexamethasone, ondansetron 4. Chronic use/ recent administration of antiemetic drugs within 24 h 5. Impaired liver (> Child-Pugh class B) or kidney function (eGFR < 30 mL/min/1.73m2) 6. Pregnancy 7. BMI <18-35 > mg/m2 8. Emergency surgery 9. Unstable hemodynamics

Design outcomes

Primary

MeasureTime frame
Incidence and episodes of nausea and vomiting At first 1 hr, At 1 - 24 hr patient report e.g Nausea/Vomiting (N/V) score (0-3)

Secondary

MeasureTime frame
Severity of postoperative nausea and vomiting 1st to the 24th hour postoperatively observe patient clinical ,amount of requested antiemetic 1st to the 24th hour postoperative medical record , amount of requested opioid drugs. 1st to the 24th hour postoperative medical record ,Times from reversal to Extubation emergence phase observe clinical patient ,Times from reversal to Eye opening to command emergence phase observe clinical patient ,Times from reversal to Purposeful responses to verbal command emergence phase observe patient clinical ,Hypotension intraoperative anesthetic record ,Awareness intraoperative Patient reported ,Brain edema intraoperative report by surgeon,Patient satisfaction at 24 hour postoperative Patient reported outcome using a questionnaire interview

Countries

Thailand

Contacts

Public ContactPimol Laohawee

Department of Anesthesiology, Faculty of Medicine, Khon Kaen University

pimol.l@kkumail.com0829544266

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026