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Reduction of the anterior shoulder dislocation with three different methods

The new FARES (FAst REliable Safe) method of reduction of the acute anterior dislocation of the shoulder: a prospective randomised comparative study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN80984121
Enrollment
144
Registered
2009-02-27
Start date
2006-09-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Traumatic shoulder dislocation Musculoskeletal Diseases Dislocation, sprain and strain of joints and ligaments of shoulder girdle

Interventions

Participants were randomly allocated to the following three arms: 1. The FARES method 2. The "Hippocrates" method 3. The "Kocher" method Duration of treatment for each participant was up to 10 min i

Sponsors

Aristotle University of Thessaloniki (Greece)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adults (>18 years old), both males and females 2. Patients suffering from 'first-time' traumatic anterior dislocation of the shoulder (either accompanied by a fracture of the greater humeral tuberosity or not)

Exclusion criteria

Exclusion criteria: 1. Patients suffering from voluntary and/or recurrent dislocation or reporting prior episode(s) of subluxation 2. Patients suffering from dislocation associated with 3- or 4-parts fracture of the proximal humerus 3. Patients with duration of dislocation greater than 24 hours 4. Intoxicated patients 5. Patients that had used any analgesics and/or muscle relaxants before attempting reduction

Design outcomes

Primary

MeasureTime frame
Efficacy of each individual method as far as the reduction of the shoulder dislocation was concerned. The efficacy was validated by x-rays following the reduction attempt and by the ability of the patient to perform voluntary and painless movements of the affected arm.

Secondary

MeasureTime frame
1. Evaluation of the pain felt during the reduction, measured using the Visual Analogue Scale (VAS) score (0 = no pain, 10 = unbearable pain) 2. Evaluation of the existence of any immediate complication following the reduction of the shoulder dislocation

Countries

Greece

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026