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Study to investigate the behaviour of paracetamol in the body of patients over 80 years old admitted to an acute geriatric ward

Phase 1
Conditions
PyrexiaPain
Therapeutic area: Diseases [C] - Symptoms and general pathology [C23]
Registration Number
EUCTR2015-004217-24-BE
Lead Sponsor
Z Leuven
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

80 years or older
Admitted to acute geriatric ward of University Hospitals Leuven
Oral intake of Dafalgan (paracetamol) tablets, 3 times 1 gram per day for at least 4 intakes before inclusion
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) no
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 40

Exclusion Criteria

Downgrading of care in terms of palliative situation

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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