BridgeMD
Compares treatment options for Rotator Cuff Syndrome
Official title Study Comparing Two Anesthetics for Arthroscopic Rotator Cuff Repair
ClinicalTrials.gov ID: NCT07093905
What this study is testing
- What it's testing
- The purpose of this study is to to compare the post-anesthetic recovery time to awake consciousness and hemodynamic and ventilatory capacities for discharge from the Post-Interventional Monitoring Room in patients admitted for shoulder rotator cuff arthroscopy (using local anesthesia versus general anesthesia + local anesthesia).
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Age ≥ 18 years;
- Patients with surgically repairable complete or partial rotator cuff tears;
- American Society of Anesthesiologists Class I to III;
- Patient able to understand study information;
- Patient willing to accept study evaluations and follow-up visits;
You likely can't join if
- Contraindication to general or locoregional anesthesia;
- Chronic opioid use;
- Patient unable to understand study information (linguistic, psychological, cognitive, etc.);
- Patient unable to answer a self-questionnaire;
- Patient participating in or being excluded from another treatment research study;
- Pregnant or breast-feeding women;
See the full eligibility criteria
- Age ≥ 18 years;
- Patients with surgically repairable complete or partial rotator cuff tears;
- American Society of Anesthesiologists Class I to III;
- Patient able to understand study information;
- Patient willing to accept study evaluations and follow-up visits;
- Affiliation with a social insurance plan;
- Patient having been informed and having agreed to participate in the study by signing an informed consent form.
- Contraindication to general or locoregional anesthesia;
- Chronic opioid use;
- Patient unable to understand study information (linguistic, psychological, cognitive, etc.);
- Patient unable to answer a self-questionnaire;
- Patient participating in or being excluded from another treatment research study;
- Pregnant or breast-feeding women;
- Protected patient (under legal protection, guardianship or deprived of liberty by judicial or administrative decision).
The study team makes the final eligibility decision.
Where it's taking place
- Marseille, France
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Marseille, France. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.