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Clinical Trials/NCT03815799
NCT03815799
Completed
Not Applicable

The Effect of Ultrasound-Guided Erector Spinae Block on Respiratory Function After Laparoscopic Cholecystectomy

Konya Meram State Hospital1 site in 1 country68 target enrollmentMarch 3, 2019
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ConditionsLaparoscopic CholecystectomyPostoperative PainRespiratory Function

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Laparoscopic Cholecystectomy
Sponsor
Konya Meram State Hospital
Enrollment
68
Locations
1
Primary Endpoint
Scoring of postoperative pain
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The aim of this study is to assess the effect of ultrasound guided erector spinae block in control of the postoperative pain and the respiratory functions after laparoscopic cholecystectomy.

Registry
clinicaltrials.gov
Start Date
March 3, 2019
End Date
September 30, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Asst. Prof. Munıse Yıldız M.D.

Ass.Prof.

Konya Meram State Hospital

Eligibility Criteria

Inclusion Criteria

  • •American Society of Anesthesiology (ASA) physical status I-II patients who were scheduled for elective laparoscopic cholecystectomy

Exclusion Criteria

  • •Patients refusal
  • •Contraindications for regional anesthesia
  • •Alcohol or drug abuse
  • •Chronic opioid intake
  • •Patient with psychiatric disorders
  • •Use of pain killers within the 24 h before the operation
  • •Respiratory tract infection within the last 2 weeks
  • •Smoker or history of smoking
  • •Allergy to local anesthetics
  • •Respiratory and allergic diseases

Outcomes

Primary Outcomes

Scoring of postoperative pain

Time Frame: Postoperative 24 hour

The primary outcome variable is Numeric Rating Scale (NRS) pain scores changes both at rest and movement. NRS use numbers to rate pain from 0 (no pain) to 10 (worst pain).

Secondary Outcomes

  • Analgesic consumption(Postoperative 24 hour)
  • Spirometric Parameters of Respiratory Functions(Preoperative (before the surgery) and at postoperative 24th hour)
  • Number of Adverse events(Postoperative 24 hour)

Study Sites (1)

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