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NCT06260137 Clinical Trial

Comparison of Two Different Methods for Reducing Pain After Lung Surgery

Postoperative Analgesia Clinical Trial

Official title:
Comparison of the Effectiveness of the Combination of Rhomboid Intercostal and Sub-serratus Plan Block and Rhomboid Intercostal Block for Postoperative Analgesis in Video-assisted Thoracopic Surgery (VATS)

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT06260137
Other study ID # UludagThorax
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date July 10, 2023
Est. completion date August 2024

Study information
Verified date February 2024
Source Uludag University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical study is to compare the effectiveness of the Rhomboid Intercostal Block and Sub-Servitus plan block and the effectiveness of the Rhomboid intercostal block in patients with video-supported thoracoscopic surgery. The main question it aims to answer is: Which of these two blocks more effectively reduces the patients' pain?

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 60
Est. completion date August 2024
Est. primary completion date July 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Patients in American Society of Anesthesiologists (ASA) classes I, II and III for whom VATS is planned Exclusion Criteria: - Known or suspected local anesthetic allergy - coagulopathy - injection site infection - history of thoracic surgery - serious neurological or psychiatric disorder - severe cardiovascular disease - liver failure - renal failure

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Rhomboid intercostal block
Patients will be injected with a local anesthetic drug under the rhomboid intercostal muscle before surgery.
• Rhomboid intercostal and subserratus plane block
Patients will be injected with a local anesthetic drug under the rhomboid intercostal muscle and the serrates anterior muscle before surgery.

Locations
Country Name City State
Turkey Hastane Bursa

Sponsors (1)
Lead Sponsor Collaborator
Uludag University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Postoperative analgesia Patients' VAS scores and additional analgesic needs in the first 48 hours will be evaluated. VAS (visual pain scale) corresponds to a value between 0 and 10. A value of 0 means no pain, and a value of 10 is the most severe pain. first 48 hours postoperatively
See also
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