Status:
COMPLETED
Effecot of Serratus Posterior Superior Intercostal Plane Block and Thoracic Paravertebral Block in VATS
Lead Sponsor:
Hitit University
Collaborating Sponsors:
Ankara Ataturk Sanatorium Training and Research Hospital
Conditions:
Video-assisted Thoracoscopic Surgery
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
Video-assisted thoracoscopic surgery (VATS) has become a standard procedure in both minor and major lung surgeries in thoracic surgery operations. Although postoperative pain in patients undergoing VA...
Detailed Description
VATS (Video-Assisted Thoracoscopic Surgery) is based on the principle of performing surgical procedures through two 2-3 cm skin incisions into the thorax with instruments inserted through an endocamer...
Eligibility Criteria
Inclusion
- A minimum of 70 patients who will undergo VATS surgery,
- American Society of Anesthesiologists (ASA) physical classification 1-2-3,
- Aged between 18-65,
- Who have read and accepted the voluntary informed consent form,
- Body mass index (BMI) of \<35.
Exclusion
- Patients who refuse to participate in the study,
- BMI \>35,
- ASA physical classifications 4-5,
- Patients unable to perform pain scoring using the NRS system,
- Those allergic to the administered local anesthetic and designated analgesic medication, individuals declaring pregnancy or lactation,
- Patients under 18 or over 65 years of age,
- Uncontrollable anxiety,
- Alcohol and drug addiction,
- Neuromuscular and peripheral nerve diseases,
- Using high doses of opioid medication three days before surgery,
- Widespread chronic pain,
- Diabetes mellitus,
- Hepatic and renal insufficiency,
- Coagulation disorders,
- Using anticoagulant drugs,
- Infection at the site of peripheral block needle insertion,
- History of abdominal surgery or trauma,
- Unable to communicate in Turkish,
- Patients experiencing technical problems while using patient-controlled analgesia,
- Patients for whom the surgical procedure needs to be terminated for any reason before completion, as well as those for whom postoperative extubation is not planned, will not be accepted into the study.
Key Trial Info
Start Date :
January 31 2024
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 15 2024
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT06219369
Start Date
January 31 2024
End Date
August 15 2024
Last Update
January 6 2025
Active Locations (1)
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1
Hitit university
Çorum, Çorum, Turkey (Türkiye), 19100