Efficacy of Sacral Erector Spinae Plane Block (SESPB) on Postoperative Pain and Catheter-related Bladder Discomfort - Trial NCT06127394
Access comprehensive clinical trial information for NCT06127394 through Pure Global AI's free database. This phase not specified trial is sponsored by Giresun University and is currently Recruiting. The study focuses on Pain, Postoperative. Target enrollment is 54 participants.
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Study Focus
Sponsor & Location
Giresun University
Timeline & Enrollment
N/A
Nov 12, 2023
Jan 15, 2024
Primary Outcome
Catheter related bladder discomfort, 0:no discomfort 4:worst discomfort
Summary
The goal of this clinical trial is to evaluate the catheter related bladder discomfort in
 patients who will undergoing TUR-P operation. The main questions it aims to answer are:
 
 - Is sacral ESPB effective on the pudendal nerve dermatome?
 
 - Is sacral ESPB as useful as pudendal block on CRBD? Participants will be divided into
 two groups and the first group will receive sacral espb after TUR-p operation and the
 second group will receive pudendal block. Investigators will be present for 24 hours
 
 - catheter related bladder discomfort
 
 - post-operative pain,
 
 - additional analgesic needs will be questioned and the difference between the two
 groups will be evaluated.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06127394
Non-Device Trial