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Clinical Trials/NCT06177652
NCT06177652
Completed
Not Applicable

Comparison of Thoracal Paravertebral Block and Serratus Plan Block in Pain Management After Thoracotomy

Kocaeli University2 sites in 1 country58 target enrollmentJune 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Kocaeli University
Enrollment
58
Locations
2
Primary Endpoint
Morphin consumption
Status
Completed
Last Updated
last year

Overview

Brief Summary

Thoracotomy is among the most painful surgical procedures and can cause severe pain. Postoperative pain causes many complications. Therefore, pain management is important in patients undergoing thoracotomy. For this purpose, systemic analgesics are used along with ultrasound-guided nerve blocks in thoracotomy pain. The effectiveness of thoracic paravertebral block and serratus plane block in the treatment of post-thoracotomy pain will be evaluated by comparing their effectiveness and complications on postoperative pain. Since the epidural spread of the thoracic paravertebral block is more effective, the effectiveness of postoperative pain relief will be more effective

Detailed Description

Thoracotomy is among the most painful surgical procedures and can cause severe pain. This pain causes postoperative complications in patients who have thoracotomy surgery. Uncontrolled pain can cause respiratory and thromboembolic events. Therefore, effective pain management is important in patients undergoing thoracotomy. Investigators aim to compare the analgesic effectiveness and complications of thoracic paravertebral block and serratus anterior plane block in relieving thoracotomy pain, which is one of the most painful surgical procedures. It is aimed to compare the effectiveness and complications of thoracic paravertebral block and serratus plane block in postoperative pain control after thoracotomy. Providing pain control reduces postoperative complications and reduces hospital stay, which increases patient comfort and reduces costs. In this research, postoperative morphine consumption after block applications will be compared, and patients' analgesic needs will be evaluated according to the participants' VAS score. Post-operative 3rd, 6th, 9th, 12th, 24th. Morphine consumption will be evaluated by monitoring the hours. It will be evaluated whether there is a need for additional analgesics. During the operation, the patient's heart rate, blood pressure, saturation and temperature variable values will be closely monitored. Standard monitoring methods will be used when examining these parameters.

Registry
clinicaltrials.gov
Start Date
June 1, 2022
End Date
July 4, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nur Nazire Yucal

Doctor

Kocaeli University

Eligibility Criteria

Inclusion Criteria

  • 18-75 aged patients
  • American Society of Anesthesiologists Classification (ASA) I-II-III patients
  • patients who scheduled elective thoracic surgery

Exclusion Criteria

  • American Society of Anesthesiologists Classification (ASA) IV-V patients
  • patients with coagulopathy
  • patient with infection at the injection site

Outcomes

Primary Outcomes

Morphin consumption

Time Frame: during postoperative 24 hour

Patient in both groups will provide with intravenous patient-controlled analgesia device containing morphine for postoperative analgesia

Secondary Outcomes

  • Visual Analogue Scale (VAS)(during postoperative 24 hour)

Study Sites (2)

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