Interest of Soft Point Anesthesia in Association With Locoregional Anesthesia in Arthroscopic Shoulder Surgery

N/ANot Yet RecruitingNCT06641167

GCS Ramsay Santé pour l'Enseignement et la Recherche96 enrolled

Overview

This is a prospective, single-center, observational study. The inclusion period is set at 12 months.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Anesthesia, Local

Interventions

Shoulder surgeryPROCEDURE

shoulder surgery by arthroscopic approach under locoregional anesthesia combining an interscalene block and a superficial cervical plexus block

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Hôpital privé Claude Galien

Quincy-sous-Sénart, France

Outcomes

Primary Outcomes

Soft point position

The primary outcome is the position of the soft point in relation to the anesthetized area mapped by loco-regional anesthesia

Time frame: Hour 24

Secondary Outcomes

Incision pain

Assessment of incision pain using a simple numerical scale (NRS) from 0 (no pain/not uncomfortable) to 10 (worst possible pain/most uncomfortable)

Time frame: Hour 24

Postoperative pain

Assessment of postoperative pain using a simple numerical scale (NRS) from 0 (no pain) to 10 (worst possible pain)

Time frame: Hour 2

Postoperative pain

Assessment of postoperative pain using a simple numerical scale (NRS) from 0 (no pain) to 10 (worst possible pain)

Time frame: Hour 6

Postoperative pain

Assessment of postoperative pain using a simple numerical scale (NRS) from 0 (no pain) to 10 (worst possible pain)

Time frame: Hour 24

Sedative medication

Amount of sedative medication administered

Time frame: Hour 24

Analgesic consumption

Amount of analgesics consumed within the 24 hours following surgery

Time frame: Hour 24

Intervention duration

Duration of the procedure and stay in the Post anesthesia care unit (the procedure duration is defined as the time between the start of the incision and the end of suturing)

Central Contacts

Yoann ELMALEH, MD

CONTACT

01 69 39 15 53 yoann.d.elmaleh@gmail.com

Data from ClinicalTrials.gov

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