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

NCT06127394 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2024-05-17

No results posted yet for this study

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.

Conditions

  • Pain, Postoperative

Interventions

PROCEDURE

Sacral ESP Block

Sacral ESPB median approach, 40 ml %0,25 Bupivacaine

PROCEDURE

Pudendal Block

Bilateral pudendal block, 10 ml %0,25 bupivacaine

Sponsors & Collaborators

  • Giresun University

    lead OTHER

Principal Investigators

  • Bilge Olgun Keleş · Giresun University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-12
Primary Completion
2023-12-15
Completion
2023-12-15

Countries

  • Turkey (Türkiye)

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06127394 on ClinicalTrials.gov