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Clinical Trials/NCT01549405
NCT01549405
Completed
Not Applicable

Ultrasound-Guided Intercostal Nerve Block for Postoperative Pain Relief in Percutaneous Nephrolitotomy

Diskapi Teaching and Research Hospital1 site in 1 country40 target enrollmentFebruary 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nerve Block, Intercostal Nerve
Sponsor
Diskapi Teaching and Research Hospital
Enrollment
40
Locations
1
Primary Endpoint
Postoperative Analgesic (Tramadol) Consumption
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

Percutaneous nephrolitotomy (PCNL)is an endourological procedure for the management of patients with renal calculi. Postoperative pain around the surgical area and the nephrostomy tube can being a problem. We hypothesized that intercostal nerve block at 11th and 12th rib level would alleviate postoperative pain and reduce analgesic consumption.

Detailed Description

Patients admitted for the removal of renal stones by PCNL will included in this study.Primary outcome measure will be analgesic (tramadol )consumption and visual analog scale (VAS).

Registry
clinicaltrials.gov
Start Date
February 2012
End Date
August 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

derya özkan

Consultant of Anesthesiology ,MD

Diskapi Teaching and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients admitted for the removal of renal stones by percutaneous
  • nephrolithotomy (PCNL)
  • ASA I-II status

Exclusion Criteria

  • Respiratory or cardiac disfunction
  • Neuropathy
  • Coagulopathy
  • BMI (Body mass index)over 30

Outcomes

Primary Outcomes

Postoperative Analgesic (Tramadol) Consumption

Time Frame: Postoperative 24th hour

Total consumption of tramadol will be measured for the first 24 hours.

Total Consumption of Tramadol Will be Measured for the First 24 Hours

Time Frame: Postoperative 24th hour

Secondary Outcomes

  • Postoperative Pain Will be Evaluated.(24 hours)

Study Sites (1)

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