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Efficacy of Transversus Abdominis Plane Block for Acute Postoperative Pain Relief in Kidney Recipients, a Double Blinded Clinical Trial

Phase 2
Conditions
kidney recipiet,s patients.
kidney transplant status
Registration Number
IRCT201012185264N3
Lead Sponsor
Vice Chancellor for research,Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
44
Inclusion Criteria

1) ASA class II and III patients
2) Aged 15–65 year who were scheduled as kidney recipients under general anesthesia
Exclusion criteria:
1)Addiction to opioids
2) Long term usage of antidepressants, antipsychotics, anticonvulsants, clonidine
3) Patients with coagulopathy and hepatomegaly.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postoperative pain. Timepoint: at 1st , 4th , 8th , 12th and 24h following surgery. Method of measurement: numeric rating scale.
Secondary Outcome Measures
NameTimeMethod
Intraoperative and first 24 hours opioids consumption. Timepoint: At the end of operation and end of first 24 hours after operation. Method of measurement: Dose calculation in mg.
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