EUCTR2014-000470-19-BE
Active, not recruiting
Phase 1
comparative study between conventional epidural versus ambulatory epidural: effect during labor in pregnant women - ambulatory epidural
Centre Hospitalier Universitaire Brugmann0 sites350 target enrollmentMarch 12, 2014
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- a single fetus pregnancy over 36 weeks and less than 42 weeks in adult nulliparous
- Sponsor
- Centre Hospitalier Universitaire Brugmann
- Enrollment
- 350
- Status
- Active, not recruiting
- Last Updated
- 8 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Free written consent.
- •Parturient aged 18\-40 years, nulliparous, ASA I or II, and singleton pregnancy over 36 weeks fetus in cephalic position, cervical dilatation between 3\-6 cm and VAS\> 30 mm, no objections for epidural
- •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 350
- •F.1\.3 Elderly (\>\=65 years) no
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •Multiparous, twin pregnancy, less than 36 weeks and over 42 weeks, the fetus in the breech position, previous history of caesarean / instrumentation, analgesia or sedation within 6h, contraindications to epidural
Outcomes
Primary Outcomes
Not specified
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