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Clinical Trials/EUCTR2006-004053-20-IE
EUCTR2006-004053-20-IE
Active, not recruiting
Not Applicable

Determination of the efficacy of the Transversus Abdominis Plane (TAP) Block in the management of postoperative pain following Caesarean Section. - TAP post LSCS

Dept of Anaesthesia, University College Hospital, Galway0 sitesSeptember 20, 2006
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ConditionsPost operative painMedDRA version: 8.1Level: LLTClassification code 10054711Term: Postoperative pain
DrugsNaropin

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post operative pain
Sponsor
Dept of Anaesthesia, University College Hospital, Galway
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 20, 2006
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
Dept of Anaesthesia, University College Hospital, Galway

Eligibility Criteria

Inclusion Criteria

  • •Adult Females aged \>18 years old
  • •Presenting for elective or emergent Caesarean Section
  • •Written Informed Consent
  • •ASA Grade 1 to 3
  • •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
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •Patient refusal
  • •Severe Pregnancy related diseases such as Pre\-Eclamsia, HELLP.
  • •Outside Age Range
  • •Allergy to bupivacaine, morphine, paracetamol, diclofenac sodium
  • •Skin lesions/infection at site of injection
  • •Renal or other organ dysfunction

Outcomes

Primary Outcomes

Not specified

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