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Clinical Trials/NCT04420104
NCT04420104
Unknown
Not Applicable

Errector Spinae Plane Block for Postoperative Pain Management in Cardiac Surgery: A Randomized Controlled Trial

Aydin Adnan Menderes University1 site in 1 country40 target enrollmentJune 1, 2020

Overview

Phase
Not Applicable
Intervention
erector spinae plane block
Conditions
Erector Spinae Plane Block
Sponsor
Aydin Adnan Menderes University
Enrollment
40
Locations
1
Primary Endpoint
change from baseline in pain the 10 point Visual Analog Scale (VAS) at hours 3,6,9,12,24,36,48.
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to assess efficacy of erector spinae plane block (ESP) for postoperative pain management in cardiac surgery patients.

Detailed Description

After being informed about the study and potential risks, all patients giving written informed consent will be randomised (single blind) as block group(patients is performed esp block) and control group. All patients will be evaluate during 48 hours for postoperative pain.

Registry
clinicaltrials.gov
Start Date
June 1, 2020
End Date
June 1, 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Aydin Adnan Menderes University
Responsible Party
Principal Investigator
Principal Investigator

SINEM SARI

Assoc. Prof. Dr.

Aydin Adnan Menderes University

Eligibility Criteria

Inclusion Criteria

  • Must be ASA score I-III
  • Must be 18-75 years old
  • must undergo cardiac surgery

Exclusion Criteria

  • emergency surgery,
  • bleeding diathesis,
  • presence of contraindications to LA agents used in this study,
  • use of chronic opioids,
  • psychiatric disorders.
  • prolonged extubation
  • presence of infection at the injection site.
  • cardiovascular conditions (EF\<40, LMCA obstruction)

Arms & Interventions

esp block group

Intervention: erector spinae plane block

esp block group

Intervention: iv analgesia

control group

Intervention: iv analgesia

Outcomes

Primary Outcomes

change from baseline in pain the 10 point Visual Analog Scale (VAS) at hours 3,6,9,12,24,36,48.

Time Frame: baseline and hours 3-6-12-24-36-48

The VAS is validated instrument assessing average pain. Possible scores range from 0 (no pain) to 10 (worst possible pain) Change= (hours 3,6,9,12,24,48 score- baseline)

time to mobilize the patient

Time Frame: Any time for 7 days

time to mobilize the patient is reported as when the patient is mobilized

Study Sites (1)

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