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Diaphragmatic Effects of Combined Infraclavicular Brachial Plexus Block and Suprascapular Nerve Block

Evaluation of the Effects of Combined Infraclavicular Brachial Plexus Block and Suprascapular Nerve Block on the Diaphragm in Arthroscopic Shoulder Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07640464
Acronym
ICB-SNB
Enrollment
61
Registered
2026-06-10
Start date
2025-02-22
Completion date
2025-07-20
Last updated
2026-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthroscopic Shoulder Surgery, Diaphragmatic Excursion, Hemidiaphragmatic Paralysis

Keywords

Anterior Suprascapular Nerve Block, Infraclavicular Brachial Plexus Block, Diaphragmatic Excursion, Shoulder Arthroscopy, Regional Anesthesia

Brief summary

This prospective observational study was conducted to evaluate the effects of a combined infraclavicular brachial plexus block and anterior suprascapular nerve block on diaphragmatic function in patients undergoing arthroscopic shoulder surgery. A total of 61 adult patients were enrolled in the study. Diaphragmatic excursion was assessed using ultrasonography both prior to block administration and 30 minutes following the procedure during normal and deep breathing. The primary objective was to assess changes in diaphragmatic excursion and determine the incidence of hemidiaphragmatic paralysis associated with this combined block technique. Secondary outcomes included block performance time, duration of postoperative analgesia, the need for additional intraoperative sedation or analgesia, the occurrence of adverse events, and levels of patient and surgeon satisfaction. The study sought to determine whether this regional anesthesia approach could provide effective anesthesia and analgesia while minimizing impairment of diaphragmatic function.

Detailed description

This prospective observational study was conducted to evaluate the effects of combined infraclavicular brachial plexus block and anterior suprascapular nerve block on diaphragmatic excursion in patients undergoing elective arthroscopic shoulder surgery. Patients scheduled for arthroscopic shoulder surgery under regional anesthesia were enrolled in the study. Prior to block administration, baseline diaphragmatic excursion was assessed using ultrasonography during both normal and deep breathing. Each measurement was repeated three times, and the mean value was recorded. The same measurements were repeated 30 minutes after completion of the block procedures using an identical protocol. The percentage change in diaphragmatic excursion between baseline and post-block measurements was calculated for both normal and deep breathing. Hemidiaphragmatic paralysis was categorized according to the degree of reduction in diaphragmatic excursion as absent (≤25% reduction), partial (25.1-74.9% reduction), or complete (≥75% reduction). All nerve blocks were performed under ultrasound guidance by anesthesiologists experienced in regional anesthesia techniques. The infraclavicular brachial plexus block was performed using 15 mL of 0.5% bupivacaine deposited around the posterior cord and 8 mL of 0.5% bupivacaine around the lateral cord. The anterior suprascapular nerve block was performed with 7 mL of 0.5% bupivacaine. In addition, arthroscopic portal sites were infiltrated with 10 mL of 0.2% bupivacaine to provide supplementary analgesia. All patients received intravenous midazolam (2 mg) and paracetamol (1 g) during the intraoperative period. Additional analgesic or sedative medication was administered when required according to clinical conditions and surgical needs. Block performance time, requirement for supplemental analgesia or sedation, and any block-related adverse events were recorded. The primary outcome measure was the change in diaphragmatic excursion measured by ultrasonography 30 minutes after block administration. Secondary outcome measures included the incidence and severity of hemidiaphragmatic paralysis, block performance time, duration of postoperative analgesia, need for additional intraoperative analgesia or sedation, time to first analgesic requirement, patient and surgeon satisfaction, block-related complications, and conversion to general anesthesia. The study was designed to investigate whether the combination of infraclavicular brachial plexus block and anterior suprascapular nerve block could provide effective anesthesia and analgesia for arthroscopic shoulder surgery while minimizing impairment of diaphragmatic function and reducing the incidence of clinically significant hemidiaphragmatic paralysis.

Interventions

None listed

Sponsors

Gazi University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged 18-80 years. * ASA physical status I-III. * Scheduled for elective arthroscopic shoulder surgery. * Ability to provide written informed consent

Exclusion criteria

* Refusal to undergo peripheral nerve block. * Pre-existing peripheral neuropathy. * Known pulmonary, hepatic, or renal disease. * Allergy to local anesthetics. * Infection at the block site. * Pre-existing neurological deficit. * Body mass index (BMI) \> 40 kg/m². * Coagulopathy. * Sepsis. * Previous surgery at the planned block site. * Major psychiatric disorders. * Inability to complete diaphragmatic ultrasonographic assessment.

Design outcomes

Primary

MeasureTime frameDescription
Change in Diaphragmatic Excursion at 30 Minutes After Block Administration30 minutes after block administrationDiaphragmatic excursion measured by ultrasonography during normal and deep breathing before block administration and 30 minutes after block administration. The percentage change from baseline was calculated.

Secondary

MeasureTime frameDescription
Incidence of Hemidiaphragmatic Paralysis30 minutes after block administrationPresence of hemidiaphragmatic paralysis determined by ultrasonographic assessment of diaphragmatic excursion.
Degree of Hemidiaphragmatic Paralysis30 minutes after block administrationHemidiaphragmatic paralysis classified as absent (≤25% reduction), partial (25.1-74.9% reduction), or complete (≥75% reduction)
Block Performance TimeFrom needle insertion to completion of the block procedureTime required to complete the combined infraclavicular brachial plexus block and anterior suprascapular nerve block.
Additional Intraoperative Analgesia RequirementFrom surgical incision to the end of surgeryRequirement for supplemental analgesic medication during surgery.
Time to First Analgesic RequirementUp to 24 hours after surgeryTime from completion of the block procedure to the first postoperative analgesic request.
Block-Related ComplicationsFrom block administration until 24 hours after surgeryIncidence of block-related adverse events including Horner syndrome, hoarseness, nausea/vomiting, and hemodynamic complications.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORIRFAN GUNGOR, MD

Gazi university faculty of medicine

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 11, 2026