NCT06127394

Efficacy of Sacral Erector Spinae Plane Block (SESPB) on Postoperative Pain and Catheter-related Bladder Discomfort

Name: Clinical Trial NCT06127394
Creator: Giresun University
Keywords: Pain, Postoperative, Sacral ESP Block, procedure, clinical trial, Turkey

Comparison of the Efficacy of Sacral Erector Spinae Plane Block (SESPB) and Pudendal Block on Postoperative Pain and Catheter-related Bladder Discomfort (CRBD) in Patients Undergoing Trans-urethral Resection of the Prostate (TUR-P).

Giresun University·ClinicalTrials.gov·procedureRecruiting

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Study focus

Disease/Condition: Pain, Postoperative
Drug/Device/Intervention: Sacral ESP Block
Study type: Interventional
Intervention type: procedure

Sponsor & location

Primary sponsor: Giresun University
Location: Merkez, Turkey

Timeline & enrollment

Phase: N/A
Start date: Nov 12, 2023
End date: Jan 15, 2024
Enrollment: 54 participants

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

During surgical operationDuring surgical operationDuring surgical operationPain, unspecifiedPostoperative intestinal obstruction

Data source

Registry: ClinicalTrials.gov
Trial ID: NCT06127394
Type: Non-Device Trial

About this record

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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