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Effect of Dexamethasone Adjuvant in Combined Supraclavicular Block and Suprascapular Block Versus Interscalene Block in Patients Undergoing Shoulder Arthroscopy

Not Applicable
Recruiting
Conditions
Shoulder Arthroscopy Blocks
Dexamethasone
Interventions
Procedure: Shoulder arthroscopy blocks
Registration Number
NCT06262893
Lead Sponsor
Assiut University
Brief Summary

In this study the investigators aim to compare the effect of the suprascapular- supraclavicular nerve block in association with dexamethasone to that of the interscalene brachial plexus block on analgesic effect during arthroscopic shoulder surgery, as postoperative pain scores ,postoperative consumption of analgesic rescue medications and diaphragmatic excursion assessment.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • ASA status 1,2.

    • Age 18 years or older
    • Elective shoulder arthroscopic surgery under general anesthesia and nerve block performed preoperatively.
Exclusion Criteria
  • • Patient refusal

    • Serious cardiac arrhythmias (including atrial fibrillation) or unstable coronary artery disease.
    • Use of drugs that act on the autonomic nervous system (including β- blockers).
    • Coagulation disorders..
    • Anatomical disorders and/or neuropathic disease.
    • BMI above 40.
    • History of substance abuse.
    • Chronic use of psychotropic and/or opioid.
    • History of psychiatric diseases needing treatment.
    • Allergy to any drug in the study protocol.
    • Failure of nerve block performed in the preoperative block room when tested prior to entering the operating room (i.e. lack of loss of sensation to ice at the shoulder incision level).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Interscalene block in shoulder arthroscopyShoulder arthroscopy blocks-
Combined Supraclavicular block and suprascapular block in shoulder arthroscopyShoulder arthroscopy blocks-
Primary Outcome Measures
NameTimeMethod
Postoperative analgesia by visual analog scale (VAS).48 hours

The

primary outcome of this study will be to evaluate and compare between suprascapular-supraclavicular nerve block in association with dexamethasone to that of the interscalene brachial plexus block on postoperative analgesia by vas score during 48h postoperatively ( 2h , 6h , 12h, 24h and 48h).

The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be').

Secondary Outcome Measures
NameTimeMethod
Diaphragmatic excursion1hour postoperatively

Assessment of diaphragmatic excursion by ultrasound preoperatively and 1hour postoperatively

Trial Locations

Locations (1)

Assiut University

🇪🇬

Assiut, Egypt

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