EUCTR2015-004600-30-BE
Active, not recruiting
Phase 1
Conventional patient controlled epidural analgesia (PCEA) versus programmed intermittent epidural boluses (PIEB) for labor analgesia: a randomized, double blind study in nulliparous women
niversity Hospitals Leuven0 sites125 target enrollmentNovember 19, 2015
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- providing adequate analgesia during labor and child birth
- Sponsor
- niversity Hospitals Leuven
- Enrollment
- 125
- Status
- Active, not recruiting
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Nulliparous, term, singleton pregnancies with spontaneous or induced labor
- •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 130
- •F.1\.3 Elderly (\>\=65 years) no
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •\-ASA 3, 4 and 5
- •\-Cervical dilatation \>7cm
- •\-Inability to perform evaluation
- •\-Age \<18 years
- •\-Intolerance to any of the drugs used in the study
- •\-Coagulopathy or infection
- •\-Clinical evidence of peripheral neuropathies
- •\-Refusal to sign informed consent
Outcomes
Primary Outcomes
Not specified
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