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

Conditions
Post operative pain
MedDRA version: 8.1Level: LLTClassification code 10054711Term: Postoperative pain
Registration Number
EUCTR2006-004053-20-IE
Lead Sponsor
Dept of Anaesthesia, University College Hospital, Galway
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
Female
Target Recruitment
Not specified
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
Sepsis

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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