Postoperative Analgesia
Conditions
Brief 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?
Interventions
PROCEDURERhomboid intercostal block
Patients will be injected with a local anesthetic drug under the rhomboid intercostal muscle before surgery.
Patients will be injected with a local anesthetic drug under the rhomboid intercostal muscle and the serrates anterior muscle before surgery.
Sponsors
Uludag University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Postoperative analgesia | first 48 hours postoperatively | 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. |
Countries
Turkey (Türkiye)
Outcome results
None listed