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Comparing the Incidence of Postoperative Headache Between Propofol and Sevoflurane for Maintenance of Anesthesia

A Single-Center Randomized Controlled Trial Comparing the Incidence of Postoperative Headache Between Propofol and Sevoflurane for Maintenance of Anesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1031250112
Enrollment
120
Registered
2025-05-20
Start date
2025-05-20
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Patients undergoing elective surgery under general anesthesia

Interventions

Anesthesia will be maintained with either propofol or sevoflurane according to randomized allocation.

Sponsors

Higurashi Aya
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients aged 18 to 70 years old who are scheduled for surgery and will undergo general anesthesia

Exclusion criteria

Exclusion criteria: 1) Patients with contraindications to the administration of propofol or sevoflurane 2) Patients with ASA classification of class 4 or higher, which is the general condition classification of the American Society of Anesthesiologists 3) Patients undergoing neurosurgery, spinal surgery, or head and neck surgery 4) Patients who may leave the operating room while intubated 5) Patients for whom the surgeon has specified or requested a general anesthesia method 6) Pregnant women

Design outcomes

Primary

MeasureTime frame
Presence of postoperative headache

Secondary

MeasureTime frame
Evaluate the severity of postoperative headache in 4 stages. Occurence of Postoperative nausea and vomit.

Contacts

Public ContactAya Higurashi

Yokohama City University Hospital

higurashi.aya.sc@yokohama-cu.ac.jp+81-45-787-2800

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026