Measurement of paracetamol concentration with a novel electrochemical technique from fingerprick-, saline - and urine samples.
Phase 1
- Conditions
- This is a laboratory equipment validation study. All subjects are healthy volunteered individuals.Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
- Registration Number
- EUCTR2020-002908-39-FI
- Lead Sponsor
- Helsinki University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- All
- Target Recruitment
- 12
Inclusion Criteria
Informed consent. Healthy, normal weight, age 18-45. Must pass medical examination prior to inclusion.
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 12
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Not considered healthy.
Alcohol, tobacco, or illegal substance use.
Regular medication incl contraceptives
Pregnancy, planned pregnancy or lactation
Participation in another clinical trial within 3 monts
Blood donation within 3 monts.
BMI < 18.5 or > 30
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