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Clinical Trials/EUCTR2015-001738-33-FR
EUCTR2015-001738-33-FR
Active, not recruiting
Phase 1

Programmed Intermittent Epidural Bolus versus Continuous Epidural Infusion for third trimester voluntary termination of pregnancy analgesia : a randomized study. - PCEA-IMG

CHU de LIMOGES0 sites37 target enrollmentAugust 5, 2015
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ConditionsTermination PregancyMedDRA version: 18.0Level: PTClassification code 10015011Term: Epidural anaesthesiaSystem Organ Class: 10042613 - Surgical and medical proceduresTherapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
DrugsChirocaineSufentanilCatapressan

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Termination Pregancy
Sponsor
CHU de LIMOGES
Enrollment
37
Status
Active, not recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 5, 2015
End Date
December 11, 2018
Last Updated
4 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
CHU de LIMOGES

Eligibility Criteria

Inclusion Criteria

  • •\-age \= 18 year
  • •\-ASA 1 or 2 (healthy women)
  • •\-pregnancy at third trimester
  • •\-willingness of voluntary interrupt the pregnancy
  • •\-women affiliated to french health social system
  • •\-written informed consent from every patient
  • •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 34

Exclusion Criteria

  • •\-contraindications to epidural analgesia
  • •\-opioids consumption within the last 24 hours
  • •\-patient’s unwillingness
  • •\-inability to comprehend or comply with the procedure

Outcomes

Primary Outcomes

Not specified

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