SPSIP Versus RISS Block in Volume-Preserving VATS
Recruiting
N/A
Interventional Study
Postoperative Pain
Thoracic Surgery
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 75
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 84 (estimated)
- Sponsor
- Ferit Yetik · Government
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About This Trial
This prospective randomized controlled study aims to compare the effects of Serratus Posterior Superior Intercostal Plane (SPSIP) block and Rhomboid Intercostal and Subserratus (RISS) block on postoperative pain, respiratory function, and recovery quality in patients undergoing volume-preserving video-assisted thoracoscopic surgery (VATS). Eighty-four patients will be randomized in a 1:1 ratio to …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients scheduled for elective biportal video-assisted thoracoscopic surgery (VATS) with lung parenchyma-preserving thoracic procedures under general anesthesia
* American Society of Anesthesiologists (ASA) physical status I-III
* Age between 18 and 75 years
* Provision of wr…
Contacts