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Clinical Trials/EUCTR2014-000470-19-BE
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.

Registry
who.int
Start Date
March 12, 2014
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
Centre Hospitalier Universitaire Brugmann

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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