Comparison of the Analgesic Effects of Continuous Versus Single-Shot Serratus Posterior Superior Intercostal Plane Block in Arthroscopic Shoulder Surgery
NCT ID: NCT06826846
Last Updated: 2026-01-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
90 participants
INTERVENTIONAL
2025-03-01
2025-10-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The Serratus Posterior Superior Intercostal Plane Block (SPSIPB) was first described in 2023 by Serkan Tulgar et al. Cadaveric studies and dermatomal analyses in patients have demonstrated its ability to provide analgesia in the back, neck, shoulder, axilla, and lateral thoracic regions.
Even though patients undergoing shoulder surgery benefit from the block; once the duration of a single-shot block wears off, they may experience severe pain again. The aim of this study is to investigate the analgesic effects of a single-shot SPSIPB compared to continuous infusion provided by placing a catheter in this region.
The hypothesis of this study: In arthroscopic shoulder surgery, the continuous application of the serratus posterior superior intercostal plane block using a catheter will result in lower pain scores, reduced opioid consumption, and improved patient satisfaction compared to single-shot application.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Interscalene Block Versus Serratus Posterior Superior Intercostal Plane Block for Arthroscopic Shoulder Surgery
NCT07311096
Comparison of SPSIPB With SSB and ICB Combination in Arthroscopic Shoulder Surgeries
NCT07233681
Comparison of Postoperative Analgesic Efficacy of SPSIPB and Combination of IBPB and SCPB
NCT06660875
SPSIPB vs CCB in Arthroscopic Shoulder Surgeries
NCT07259785
Serratus Posterior Superior Intercostal Plane Block for Arthroscopic Shoulder Surgery
NCT06866054
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
OTHER
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Group 1: This patient group will not undergo any regional block
No interventions assigned to this group
Group 2: Patients who will receive a single-shot serratus posterior superior plane block
Serratus posterior superior intercostal plane block (single-shot)
30 mL of 0.25% bupivacaine will be injected as single-shot block 20 mins prior to surgery
Group 3: Patients who will receive a continuous SPSIB with catheter
Serratus posterior superior intercostal plane block (catheter)
In addition to administration of 30 mL of 0.25% bupivacaine prior to surgery, a catheter will be placed in the area to administer bolus of 1 mg/kg of 0.25% bupivacaine every 8 hours postoperatively.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Serratus posterior superior intercostal plane block (single-shot)
30 mL of 0.25% bupivacaine will be injected as single-shot block 20 mins prior to surgery
Serratus posterior superior intercostal plane block (catheter)
In addition to administration of 30 mL of 0.25% bupivacaine prior to surgery, a catheter will be placed in the area to administer bolus of 1 mg/kg of 0.25% bupivacaine every 8 hours postoperatively.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* No bleeding diathesis
* Classified as ASA I-II-III
Exclusion Criteria
* Patients with coagulopathy
* History of allergy or intoxication to local anesthetic agents
* Patients with advanced organ failure
* History of neuropathic disease
* Patients with mental retardation
* Presence of infection at the injection site
* Conditions in which regional anesthesia is contraindicated
* Pediatric patients and those over 80 years of age
* Pregnant patients
18 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Goztepe Prof Dr Suleyman Yalcın City Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
ILKER YALCIN
Anesthesiology and Reanimation Resident, M.D.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Senem Koruk
Role: STUDY_DIRECTOR
Goztepe Prof Dr Suleyman Yalcın City Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Goztepe Suleyman Yalcin City Hospital
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AOSPS001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.