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Clinical Trials/NCT04235530
NCT04235530
Completed
Not Applicable

Comparison of Ultrasonography Guided Serratus Anterior Plane Block and Thoracic Paravertebral Block in Video-Assisted Thoracoscopic Surgery: A Prospective Randomized Double-blind Study

Merve Sena BAYTAR1 site in 1 country5 target enrollmentApril 15, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Merve Sena BAYTAR
Enrollment
5
Locations
1
Primary Endpoint
pain scores in rest and coughing
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The aim of this study is comparison of the effectiveness of ultrasound guided serratus anterior plane block and thoracic paravertebral block as a preventive analgesia method after VATS. Our secondary aim is to investigate patient and surgeon satisfaction, duration of block application, postoperative complications and hospital lenght of stay.

Registry
clinicaltrials.gov
Start Date
April 15, 2018
End Date
February 1, 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Merve Sena BAYTAR
Responsible Party
Sponsor Investigator
Principal Investigator

Merve Sena BAYTAR

Medical Doctor

Bursa Yüksek İhtisas Education and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • aged between 18 and 65 years
  • ASA (American Society of Anesthesiologists) score I-II

Exclusion Criteria

  • inability to communicate
  • body mass index (BMI) \> 35 kg/m2
  • infection in the area where the block was to be applied
  • allergy to the drugs used
  • mentally impaired
  • bleeding impaired

Outcomes

Primary Outcomes

pain scores in rest and coughing

Time Frame: 24 hours

Pain scores observed after surgery at 0, 1 ,2 ,6 ,12 ,24 th hours by visual analog scale. We assessed pain scores both in rest and coughing. This scale scores pain from 0 to 10. 0 means no pain and 10 means unbearable pain.

consumption of opioids

Time Frame: 24 hours

We observed how much opioid ( how many miligrams) the patient consumed in 24 hours postoperatively with pca device.

Secondary Outcomes

  • postoperative complications(24 hours)
  • lenght of hospital stay(48 hours)

Study Sites (1)

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