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Hypnosis to Reduce Pain and Drugs for Shoulder Dislocation Management

Hypnosis to Reduce Pain and Drugs for Shoulder Dislocation Management in the Emergency Department

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04992598
Acronym
HYPSEM
Enrollment
0
Registered
2021-08-05
Start date
2024-06-01
Completion date
2024-08-01
Last updated
2024-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shoulder Dislocation

Keywords

Hypnosis

Brief summary

The effectiveness of hypnosis for reducing pain was evaluated in various medical specialities. However, only few studies have demonstrated the efficacy of hypnosis for the management of pain in the emergency medicine. Anteromedial dislocation is a very common Reason for admission in emergency department. Many methods for reduction have been described but there is no consensus on the optimum technique or sedation procedures. Some pain medication and tranquilizers used during a shoulder dislocation management include hemodynamic, respiratory and behavioral adverse effects with the requirement of strengthened surveillance. Hypnosis could provide to reduce sedative and analgesic use during the reduction of anteromedial dislocation. The main objective of this study is to evaluate the efficacy of a hypnosis session for reducing the consumption of analgesic in patient throughout a reduction of shoulder dislocation. The investigators also examine the effect of hypnosis on hemodynamic parameters, patient's pain, patient and practitioner satisfaction, sedative consumption, number of attempts for reduction and length of stay in the emergency department.

Interventions

Hypnosis session will precede therapeutic strategies and reduction

PROCEDUREReduction

All dislocation would be reduced Under adequate analgesia and sufficient sedation. All methods for reduction can be used.

Sponsors

Centre Hospitalier Régional Metz-Thionville
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged 18 years and over, * Checked into ED for an anterior shoulder dislocation suspected by clinical examination and confirmed by radiography, * Had given oral consent to participate in the study * Are affiliated or be a recipient of a social security plan. * A staff member (nurse, nurse's aide, or physician) trained in hypnosis is available at the patient admission time.

Exclusion criteria

* Patient showing up with a shoulder fracture on x-ray. * Patient presenting a shoulder prosthesis. * Patient with recurrent dislocations. * Patient who does not speak or understand French language. * Patient with cognitive dysfunction. * Patient with a psychiatric history of psychosis. * Patient who is deaf or hard of hearing. * Patient under legal protection (guardianship, curatorship). * Pregnant women * Patient who already benefited of a pre-hospital reduction

Design outcomes

Primary

MeasureTime frameDescription
Analgesic consumptionDay 1Calculated as the equal dose of morphine

Secondary

MeasureTime frameDescription
Patients'satisfactionDay 1Patients'satisfaction was assessed with a Likert scale after reduction. The satisfaction was scored on 5-point Likert scale, ranging from 1 to 5 (with 1=excellent and 5=catastrophic).
Practitioners'satisfactionDay 1Practitioners'satisfaction was assessed with a Likert scale after reduction. The satisfaction was scored on 5-point Likert scale, ranging from 1 to 5 ( with 1=excellent and 5=catastrophic).
Number of attempts for reductionDay 1Number of attempts for reduction
Dose of sedative drugDay 1Dose of sedative drug
Method use for reductionDay 1Method use for reduction
Adverse eventsDay 1number of adverse events
Length of stayDay 1Length of stay in the emergency department

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026