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Clinical Trials/NCT03897933
NCT03897933
Completed
Not Applicable

Erector Spinae Plane Block for Postoperative Pain in Percutaneous Nephrolithotomy Patients: a Retrospective Study

TC Erciyes University1 site in 1 country60 target enrollmentJanuary 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Percutaneous Nephrolithotomy
Sponsor
TC Erciyes University
Enrollment
60
Locations
1
Primary Endpoint
opioid consumption
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

To evaluate the ability of Erector spina Plane block decrease postoperative pain and analgesia requirements in patients undergoing Percutaneous Nephrolithotomy.

Detailed Description

Erector spina Plane block was performed with guided ultrasound at T10 Transverse process level would lead to adequate postoperative analgesia ,in Percutaneous Nephrolithotomy surgeries.

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
February 1, 2020
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sibel Seçkin Pehlivan

Teaching Assistant

TC Erciyes University

Eligibility Criteria

Inclusion Criteria

  • ASA I- ASA II Patients

Exclusion Criteria

  • history of allergy to the study medication
  • refusal to participate

Outcomes

Primary Outcomes

opioid consumption

Time Frame: 24 hours after surgery

In the recovery room, all patients were given a patient- controlled analgesia device containing morphine 0.5 mg/ml, set to deliver a 1mg bolus dose of morphine with an 10 min lockout time and 10 mg 4 h limit.Total morphine consumption during the 24 hours postoperative period will recorded at 5 times intervals ( 2, 4, 6, 12, 24 hours).

Verbal analog Pain Scores on rest and movement

Time Frame: 24 hours after surgery

A Research assistant, blinded to the group allocation, interviewed patients and collected data at 5 times intervals ( 2, 4, 6, 12, 24, hours) in the 24 hours postoperatively. Patients were asked to rate their pain using verbal analog scale, where 0= no pain and 10= worst pain possible.

Secondary Outcomes

  • Demographic data(24 hours after surgery)
  • incidences of adverse effects (like nausea and vomiting)(24 hours after surgery)

Study Sites (1)

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