Shoulder surgery: shoulder surgery by arthroscopic approach under locoregional anesthesia combining an interscalene block and a superficial cervical plexus block
Study summary
This is a prospective, single-center, observational study. The inclusion period is set at 12 months.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Patient aged 18 years or older
* Patient informed about the study and who has not opposed the use of their personal medical data
* Patient scheduled for arthroscopic shoulder surgery
Exclusion Criteria:
* Allergy to local anesthetics or epinephrine
* Contraindications to Interscalene Block (e.g., respiratory disease, pneumothorax, pneumonectomy, phrenic or recurrent laryngeal nerve paralysis)
* Coagulation disorder
* Patients unable to understand the study information and objectives: dementia, psychosis, consciousness disorders, non-French-speaking patients
* Patients under legal protection measures (guardianship, curatorship) or deprived of liberty by judicial or administrative decision
Primary outcome measure(s)
Soft point position — Hour 24 The primary outcome is the position of the soft point in relation to the anesthetized area mapped by loco-regional anesthesia
Trial sites (1)
Facility
City
Region
Status
Hôpital privé Claude Galien
Quincy-sous-Sénart
France
More GCS Ramsay Santé pour l'Enseignement et la Recherche trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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