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The effect of the Goreisan prophylaxis on headache after the cesarean operation

The effect of the Goreisan prophylaxis on headache after the cesarean operation - Goreisan prophylaxis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000019793
Enrollment
200
Registered
2015-11-20
Start date
2016-01-01
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

headache

Interventions

The Goreisan administrated group From drinking water possible time of cesarean operation, administered Goreisan content of 3 3 days Goreisan non-administrated group

Sponsors

Tohoku University Hospital Department of Anesthesiology
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: The pregnant woman of ASA PS 1, 1E, 2, 2E were planned by epidural combination spinal anesthesia.

Exclusion criteria

Exclusion criteria: Patient having a migraine headache an allergy to cinnamon bark or the lactose intolerance symptom The patient with mental disease or a mind symptom is judged to have difficulty in trial entry. The patient who is given NSAIDS, acetaminophen before operation

Design outcomes

Primary

MeasureTime frame
headache from the operation end to a discharge

Secondary

MeasureTime frame
nuesa/vomitting, breast feeding and milking, days from the operation end to a discharge

Countries

Japan

Contacts

Public ContactHiroshi Sumida

Tohoku University Department of Anesthesiology

tthsumida@yahoo.co.jp022-717-7321

Outcome results

None listed

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