Skip to content

Kampo (saireito) for Immediate cRaniotomy Surgical headaCHE

Kampo (saireito) for Immediate cRaniotomy Surgical headaCHE - KIRSCHE Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs031220605
Enrollment
40
Registered
2023-02-01
Start date
2023-03-03
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

Patient undergoing craniotomy Cerebral aneurysm, Moyamoya disease, Intracranial tumor

Interventions

Medication: Three packets of Saireito per day, divided into three doses, are administered orally before or between meals. The administration period is one week before and one week after surgery, for a

Sponsors

Ito Yoshiro
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients undergoing craniotomy with an anterior temporal craniotomy 2) Patients who are at least 18 years old and less than 75 years old 3) Patients who have been fully informed and understood about the study, and have given written informed consent

Exclusion criteria

Exclusion criteria: 1) Patients using steroids or interleukin inhibitors 2) Female who are pregnant or may become pregnant 3) Lactating female 4) Patients who have received any other study drug or investigational drug within 3 months prior 5) Other patients who are deemed inappropriate as subjects by the investigators

Design outcomes

Primary

MeasureTime frame
Total number of analgesics used in 9-15 days (postoperative day 1-7)

Secondary

MeasureTime frame
Day 9 (postoperative day 1) (VAS, temporalis muscle swelling rate, WBC, CK, IL-6, IL-8, IL-10), Day 15 (postoperative day 7) (VAS, QoR40, pain level by Pain vision)

Contacts

Public ContactYoshiro Ito

University of Tsukuba Hospital

yoshiro@md.tsukuba.ac.jp+81-29-853-3220

Outcome results

None listed

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