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Vergelijkende studie tussen PCEA en TAP-block als postoperatieve pijnstilling bij setio-patiënte

Conditions
pain treatment after C-section
Registration Number
EUCTR2009-017326-39-BE
Lead Sponsor
niversity Hospitals Leuven
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
Female
Target Recruitment
100
Inclusion Criteria

singleton pregnancy
elective C-section
women > 18 years of age
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
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

gestational age < 36 weeks
allergy to study drug

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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