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Clinical Trials/EUCTR2015-001126-41-BE
EUCTR2015-001126-41-BE
Active, not recruiting
Phase 1

The effect of transversus abdominis plane block on postoperative analgesia after combined spinal epidural anesthesia for Cesarean delivery.

niversity Hospitals Leuven0 sitesJune 15, 2015
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Conditionsproviding adequate analgesia after cesarean delivery.Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
DrugsNaropin

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
providing adequate analgesia after cesarean delivery.
Sponsor
niversity Hospitals Leuven
Status
Active, not recruiting
Last Updated
9 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 15, 2015
End Date
TBD
Last Updated
9 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
niversity Hospitals Leuven

Eligibility Criteria

Inclusion Criteria

  • •\- obtained written consent from the patiënt.
  • •\- Patiënt presenting for elective cesarean section.
  • •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 200
  • •F.1\.3 Elderly (\>\=65 years) no
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •\- age\<18 years.
  • •\- epidural analgesia started during labour.
  • •\- preterm gestation (\<37w )
  • •\- multiple gestations
  • •\- contraindications for neuraxial anesthesia
  • •\- intolerance to any of the study drugs
  • •\- chronic steroid use
  • •\- chronic opioid use
  • •\- diabetes

Outcomes

Primary Outcomes

Not specified

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