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Clinical Trials/NCT02681471
NCT02681471
Completed
Not Applicable

Bipolar Versus Monopolar Resection of Benign Prostate Hyperplasia: A Comparison of the Effects on Plasma Electrolytes, Osmolarity and Hemoglobin

Istanbul University1 site in 1 country53 target enrollmentDecember 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Hyponatremia
Sponsor
Istanbul University
Enrollment
53
Locations
1
Primary Endpoint
Serum sodium level
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Aim of this prospective clinical study was to compare two different surgical techniques and used solutions on serum electrolytes, bleeding and Transurethral Resection of Prostate (TURP) syndrome undergoing TURP.

Fifty-three patients scheduled for elective TURP were enrolled in this prospective clinical study. Patients were included one of two groups (Group Monopolar and Group Bipolar).

Detailed Description

Background and Purpose: Aim of this prospective clinical study was to compare two different surgical techniques and used solutions on serum electrolytes, bleeding and Transurethral Resection of Prostate (TURP) syndrome undergoing TURP. Methods: Fifty-three patients scheduled for elective TURP were enrolled in this prospective clinical study. Patients were divided into two groups. Patients in Group M (Monopolar) (n=25) were used monopolar resectoscope (Karl Storz, Tottling, Germany) and 5% mannitol as irrigating solution. Patients in Group B (Bipolar) (n=25) were used bipolar resectoscope TURis (OLYMPUS, Tokyo, Japan) and isotonic saline as irrigating solution. Patients who received spinal anaesthesia were given 2.5-3 ml 0.5% hyperbaric bupivacain intrathecally and others were given general anaesthesia. Patients demographics, prostate volumes, hemodynamic parameters, volumes of irrigation and IV solutions were recorded. Blood samples were collected preoperatively (control), 45 minutes after the induction (2nd Measurement) and 1 hour after the end of the operation for analyzing serum electrolytes, osmolarity, hemoglobin values.

Registry
clinicaltrials.gov
Start Date
December 2013
End Date
April 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Meltem Savran Karadeniz

Attending Anesthesiologist

Istanbul University

Eligibility Criteria

Inclusion Criteria

  • Men were older than 50 years
  • Men suffered from symptomatic benign prostatic hyperplasia.

Exclusion Criteria

  • History of severe heart failure
  • History of respiratory failure
  • History of bleeding diathesis

Outcomes

Primary Outcomes

Serum sodium level

Time Frame: 0-3 hours

Sodium level (meq /L)

Secondary Outcomes

  • Serum osmolarity(0-3 hours)
  • Serum hemoglobin level(0-3 hours)
  • Serum potassium levels(0-3 hours)

Study Sites (1)

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