Ultrasound-Guided Serratus Posterior Superior Intercostal Plane Block for Analgesia in Arthroscopic Shoulder Surgery
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorBursa City Hospital
About this trial
This study aimed to evaluate the effectiveness of serratus posterior superior intercostal plane (SPSIP) block in managing postoperative pain in patients undergoing arthroscopic shoulder surgery.
Eligibility criteria
Qualifiers
Classified as American Society of Anesthesiologists (ASA) physical status I-II-III
Scheduled for elective shoulder arthroscopy surgery
Surgery performed under general anesthesia
Provision of written informed consent
Disqualifiers
Use of anticoagulant or antiplatelet medications
Presence of bleeding diathesis or coagulation disorders
Known allergy or hypersensitivity to local anesthetics or opioid medications
Infection or history of previous surgery at the planned block site
Trial design
Treatments tested in this trial
- Group SPSIP: Serratus Posterior Superior İntercostal Plane Block (SPSIP)
Treatment groups
80 Participants
are divided into 2 treatment groupsLocations
1Bursa City Hospital16110, Bursa Turkey (Türkiye)
Sponsors and collaborators
Bursa City Hospital
Lead sponsor
Source ClinicalTrials.gov