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Analgesic effect of continuous transversus abdominis plane block for renal transplant recipients.

Not Applicable
Completed
Conditions
Patients who are scheduled for renal transplant from living donor
Registration Number
JPRN-UMIN000013319
Lead Sponsor
Osaka University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patinets who are allergic to any medication used in the study 2. Pantients who have abdominal pain before surgery or use analgetic drugs for chronic pain 3. Patients who have severe paralysis or severe neurologic disease 4. Patients who are regarded ineligible by doctors with any other reasons

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cumulative fentanyl consumption in 48hours postoperation
Secondary Outcome Measures
NameTimeMethod
1. Visual Analogue Scale (VAS) pain scores at rest and at mobilization after 4, 16, 24, 40 and 48hours postoperation. 2. Incidence of nausea and vomitting
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