Study of the clinical outcome of Goreisan in patients with abnormal fluid retention.
Not Applicable
Recruiting
- Conditions
- Abnormal fluid retention
- Registration Number
- JPRN-UMIN000032889
- Lead Sponsor
- Tokorozawa Heart Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients younger than 20 years old 2) Patients who have allergy for cinnamon 3) Patients who are pregnant or hope to be pregnant 4) Patients who cannot take oral administration 5) Patients who have no urination due to end-stage renal failure on hemodialysis 6) Patients who are not expected to react to diuretics due to acute kidney injury 7) Patients who participate in another interventional trial 8) Patients whose doctor in charge do not agree to join the trial
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A total of 3days urine volume form the day after participation in this study.
- Secondary Outcome Measures
Name Time Method Serum creatinine, electrolyte, liver enzyme, body weight, and the degree of peripheral edema.