Clinical study of the effectiveness of Saireito on the postoperative edema after blepharoptosis surgery
Phase 2
- Conditions
- blepharoptosis
- Registration Number
- JPRN-UMIN000016258
- Lead Sponsor
- Kansai Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
*Have herbal remedy orally within 2weeks before surgery *Have any of the following systemic diseases: 1.Requiring continued use of oral corticosteroid therapy (>5 mg/day prednisolone equivalent) or immune-suppressing drug 2.malignant tumor 3.hepatuc failure or renal failure *6.Other patients judged by the investigator to be inappropriate as a subject of this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method