Epidural Anesthesia for Transurethral Resection of The Prostate

NCT06893809 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-07-25

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Summary

The aim of this study is to assess the effects of different routes of local anesthetic administration in epidural anesthesia applied to patients undergoing transurethral resection of the prostate (TUR-P). ASA I-III 60 patients were enrolled in the study. Patients were randomized into the following three groups: in Group N (needle), total dose of local anesthetic was administered through the Tuohy needle (n=20), in Group C (catheter), local anesthetic was administered through the epidural catheter (n=20) and in Group N/C (needle/catheter), local anestetic was administered half volume through the needle and half through the catheter (n=20). Hemodynamics, times to reach sensory block T10 (block levels), side effects, patient and surgeon satisfaction were evaluated.

Conditions

  • Epidural Catheter
  • Epidural Analgesia
  • Geriatric Cardiology
  • Urologic Disorders
  • Hemodynamic (MAP) Stability
  • Pain Management

Interventions

PROCEDURE

Epidural injection via Tuohy needle

Local anesthetic was administered entirely through the Tuohy needle.

PROCEDURE

Epidural injection via catheter

Local anesthetic was administered entirely through the epidural catheter.

PROCEDURE

Combined epidural injection (needle and catheter)

Half of the total local anesthetic dose was administered through the needle and half through the catheter.

Sponsors & Collaborators

  • Ankara City Hospital Bilkent

    collaborator OTHER
  • Başakşehir Çam & Sakura City Hospital

    lead OTHER_GOV

Principal Investigators

  • NERMİN GÖĞÜŞ, Prof.Dr. · Ankara City Hospital Bilkent

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
75 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-02
Primary Completion
2010-11-30
Completion
2010-12-30

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 NCT06893809 on ClinicalTrials.gov