Study of analgesic and sedative effects of suppository yokukansan for pediatric patient with postoperative tonsillectomy
Not Applicable
- Conditions
- Pediatric patient with tonsillectomy
- Registration Number
- JPRN-UMIN000013938
- Lead Sponsor
- issay Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
a) Patients who take herbal medicines b) Patients who are allergic to medicines, or foods related to the test material of this trial c) Patients who have been enrolled in the other clinical trials within last 3 months before the agreement for the participation to this trial d) Patients who are judged not suitable to participate in this trial by physician.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method