Recruiting PHASE4 Anterior Shoulder Dislocation

Compares treatment options for Anterior Shoulder Dislocation

Official title METHOXYFLURANE or Virtual Reality Headset vs Standard Analgesic Management for the Reduction of Anterior Shoulder Dislocation (HYPNOLUX)

ClinicalTrials.gov ID: NCT05821517

What this study is testing

What is Administration of METHOXYFLURANE?

Administration of METHOXYFLURANE is an investigational medicine, given as an inhaled treatment, being studied as a potential treatment for anterior shoulder dislocation.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
Anterior shoulder dislocation is a pathology frequently encountered in emergency medicine. The success in reducing anterior shoulder dislocations depends on muscle relaxation, which is itself conditioned by the patient's pain and apprehension.
  • Phase 4: studies an already-approved treatment

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

  • Pregnant and/or breastfeeding women and women of childbearing age who do not have effective contraception (hormonal, mechanical or surgical).
  • Patients with difficulties in understanding or using the devices studied.
  • Patients with a contraindication to the use of one of the studied devices.
  • Patients with a history of relevant shoulder surgery
  • Presence of other associated trauma,

You likely can't join if

  • Withdrawal of voluntary informed consent from the patient
  • Violation of protocol
  • Presence of a fracture associated with the dislocation (excluding Malgaigne's notches)
  • Posterior, inferior or erecta dislocation
  • Presence of initial vascular and nerve complications
  • Any indication for surgical management
See the full eligibility criteria
Who can join
  • Pregnant and/or breastfeeding women and women of childbearing age who do not have effective contraception (hormonal, mechanical or surgical).
  • Patients with difficulties in understanding or using the devices studied.
  • Patients with a contraindication to the use of one of the studied devices.
  • Patients with a history of relevant shoulder surgery
  • Presence of other associated trauma,
  • Previous inclusion in the same study
What rules you out
  • Withdrawal of voluntary informed consent from the patient
  • Violation of protocol
  • Presence of a fracture associated with the dislocation (excluding Malgaigne's notches)
  • Posterior, inferior or erecta dislocation
  • Presence of initial vascular and nerve complications
  • Any indication for surgical management

The study team makes the final eligibility decision.

Where it's taking place

  • Nice, France

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

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 Nice, 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.