Investigation for safety of hydrogen rich water administration to systemic inflammatory response
Phase 1
Recruiting
- Conditions
- sepsis after cardiopulmonary resuscitation
- Registration Number
- JPRN-UMIN000035141
- Lead Sponsor
- Osaka University Graduate School of Medicine Department of Traumatology and Acute Critical Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
1) Under 16 years old 2) Patients who are possible to die within 48 hours after admission 3) Patients who have gastrointestinal perforation or gastrointestinal bleeding which cannot receive tube nutrition. 4) Heart failure, stroke, respiratory failure due to COPD
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate safety, primary outcome is all adverse event including undesirable or unexpected symptoms and abnormal laboratory test value caused to the patients for one week.
- Secondary Outcome Measures
Name Time Method Changes in the intestinal flora over time