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Clinical Trials/EUCTR2008-008434-36-BE
EUCTR2008-008434-36-BE
Active, not recruiting
Not Applicable

Een gecombineerde spinale epidurale anesthesie bij arbeid : positieve invloed op kwaliteit van analgesie door epiduraal clonidine en neostigmine bij doorbraakpijn?

Marc Van de Velde0 sites100 target enrollmentJanuary 15, 2009
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ConditionsCombined spinal-epidural analgesia during labour
DrugsSufentaNaropinCatapressanProstigmin

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Combined spinal-epidural analgesia during labour
Sponsor
Marc Van de Velde
Enrollment
100
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 15, 2009
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
Marc Van de Velde

Eligibility Criteria

Inclusion Criteria

  • •ASA I or II
  • •Singleton pregnancy, vertex presented
  • •\> 37 weeks post\-conception
  • •Normal pregnancy
  • •Informed written consent
  • •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
  • •F.1\.3 Elderly (\>\=65 years) no

Exclusion Criteria

  • •ASA III and IV
  • •Maternal length \< 150 cm and BMI \> 40
  • •Suspected congenital disorder
  • •Multiple pregnancy
  • •Cervical dilatation \> 7 cm
  • •VAS \<50 mm
  • •Allergic to local anesthetics

Outcomes

Primary Outcomes

Not specified

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