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Clinical Trials/NCT03454191
NCT03454191
Terminated
Not Applicable

Efficacy of Erector Spinae Plane Block for Postoperative Analgesia in Adult Patients Undergoing Thoracoscopy

Eric Albrecht1 site in 1 country10 target enrollmentFebruary 1, 2018
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ConditionsPain, Postoperative

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Postoperative
Sponsor
Eric Albrecht
Enrollment
10
Locations
1
Primary Endpoint
IV morphine consumption
Status
Terminated
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The erector spinae plane block has been recently described as an effective analgesic postoperative pain treatment in case reports. It consists of injecting local anaesthetics below the erector spinae muscle, at the level of the transverse processes, in order to anaesthetize the thoracic roots coming out from the spinal cord. However, the analgesic efficacy has never been demonstrated in a randomized controlled trial. Therefore, the objective of this study is to investigate the analgesic benefit of this block on patients scheduled for thoracoscopy.

Registry
clinicaltrials.gov
Start Date
February 1, 2018
End Date
October 1, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Eric Albrecht
Responsible Party
Sponsor Investigator
Principal Investigator

Eric Albrecht

Program director of regional anaesthesia

Centre Hospitalier Universitaire Vaudois

Eligibility Criteria

Inclusion Criteria

  • •Patients scheduled for thoracoscopy
  • •physical status I-III

Exclusion Criteria

  • •allergy to local anaesthetics
  • •other contraindications to peripheral nerve blocks
  • •patients suffering from chronic pain condition

Outcomes

Primary Outcomes

IV morphine consumption

Time Frame: 24 postoperative hours

mg

Secondary Outcomes

  • Chronic pain scores(3 and 6 postoperative months)
  • IV morphine consumption(48 postoperative hours)
  • Pain scores(2, 24, 24 postoperative hours)
  • Forced vital capacity(24 and 48 postoperative hours)

Study Sites (1)

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