Short-term changes in pulmonary congestion depending on diuretic administration method
- Conditions
- heart failure
- Registration Number
- JPRN-jRCT1041230150
- Lead Sponsor
- Ohtani Hayato
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
1. patients between 20 and 80 years of age
2. systolic blood pressure greater than 100 mmHg and heart rate less than 100 beats/minute at the time of enrollment
3. patients who are taking 20 mg of furosemide and are not receiving intravenous diuretics
4. Patients whose consent to participate in this study has been obtained by signing a consent form by the patient or a substitute consenter.
1. patients with cardiogenic shock (with continuous catecholamine administration and mechanical circulatory support)
2. patients with serum Na concentration less than 125 mEq/l or greater than 145 mEq/l
3. patients whose participation is deemed inappropriate by the attending physician
4. dialysis patients
5. patients who have difficulty with oral fluid intake
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method