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Ultrasound Guided Pudendal Block in Transurethral Prostatectomies

NCT01501279 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2016-06-13

No results posted yet for this study

Summary

The pudendal nerve conveys sensory, motor, sympathetic fibres to the perineum, bladder neck and proximal urethra. Pain management during transurethral procedures is a major concern.Patients who have been catheterized under anesthesia complained of urgency in the postoperative period because of catheter-related bladder irritation. We want to investigate that the effect of pudendal block to postoperative pain, bladder spasm and patient comfort in transurethral prostatectomies

Conditions

  • Pain, Postoperative

Interventions

PROCEDURE

Pudendal nerve block

the pudendal nerve block is going to be performed to the medial of ischial tuberosity with USG guidance in lithotomy position

Sponsors & Collaborators

  • Diskapi Teaching and Research Hospital

    lead OTHER

Principal Investigators

  • Derya Özkan, MD · Ministry of health Diskapi Yıldirim Beyazit Training and Research Hospital 1. Anesthesiology Clinic

  • Taylan Akkaya, MD · Ministry of health Diskapi Yıldirim Beyazit Training and Research Hospital 1. Anesthesiology Clinic

  • Nihat Karakoyunlu, MD · Ministry of health Diskapi Yıldirim Beyazit Training and Research Hospital Urology Clinic

  • Julide Ergil, MD · Ministry of health Diskapi Yıldirim Beyazit Training and Research Hospital 1. AnesthesiologyClinic

  • Hamit Ersoy, MD · Ministry of health Diskapi Yıldirim Beyazit Training and Research Hospital 3. Urology Clinic

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Max Age
80 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2013-04-30
Completion
2013-04-30

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT01501279 on ClinicalTrials.gov