The ability of strong albumin solution infused intravenously to allocate fluid from the tissues to the cirkulation in healthy subjects and in burn patients
Phase 1
- Conditions
- Healthy adult volunteers and burn patients 3 to 10 Days after the injury.Therapeutic area: Body processes [G] - Physiological processes [G07]
- Registration Number
- EUCTR2016-000996-26-SE
- Lead Sponsor
- Region Ostergotland
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
Healthy volunteers
Burn patients 3 to 10 Days after the injury.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 30
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Patients with serious cardiac or pulmonary disease.
Health stats corresponding to American Society of Anesthesiologists (ASA) Group III and IV.
Inability to understand instructions.
Dementia.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method