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

Results pending

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.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-03-01

Study Completion Date

2025-10-10

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Patients undergoing arthroscopic shoulder surgery often experience moderate to severe postoperative pain. Various medical treatments are employed to provide analgesia for these patients. The advancement of regional anesthesia techniques has made possible to both reduce the use of narcotic analgesics and provide long-term pain management benefits.

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.

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.

Arthroscopic Shoulder Surgery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

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

Group Type NO_INTERVENTION

No interventions assigned to this group

Group 2: Patients who will receive a single-shot serratus posterior superior plane block

Group Type ACTIVE_COMPARATOR

Serratus posterior superior intercostal plane block (single-shot)

Intervention Type OTHER

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

Group Type ACTIVE_COMPARATOR

Serratus posterior superior intercostal plane block (catheter)

Intervention Type OTHER

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

Intervention Type OTHER

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.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Aged between 18-80 years
* No bleeding diathesis
* Classified as ASA I-II-III

Exclusion Criteria

* Patients who do not provide consent
* 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
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Goztepe Prof Dr Suleyman Yalcın City Hospital

OTHER

Sponsor Role lead

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.

Responsibility Role PRINCIPAL_INVESTIGATOR

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)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

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.

Combined SAPB in MICS
NCT06326320 COMPLETED NA
SPSIP Block and Opioid Use After MICS
NCT07259824 RECRUITING NA