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Comparison of two different methods of displacement of anterior shoulder dislocation

A comparison between the Spaso and the double traction methods for reduction of anterior shoulder dislocation in the patients admitted to emergency department : A controlled clinical trial.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20151123025202N29
Enrollment
112
Registered
2023-04-08
Start date
2023-04-04
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

shoulder dislocation. Pathological dislocation of shoulder, not elsewhere classified

Interventions

Intervention 1: Intervention group: In this group, dislocation reduction is done by double traction method. In such a way that two people stand on the side of the dislocation in such a way that one of

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Diagnosis of anterior shoulder dislocation Elapse of dislocation period less than 24 hours

Exclusion criteria

Exclusion criteria: Simultaneous fracture of the humerus Morbid obesity History of previous shoulder joint surgery Unconsciousness Impaired hemodynamics Multiple traumas Posterior shoulder dislocation

Design outcomes

Primary

MeasureTime frame
Dislocation treatment. Timepoint: After shoulder dislocation Reduction. Method of measurement: Observation shoulder X-Ray.;Pain Severity. Timepoint: During reduction of dislocation. Method of measurement: Using a 10-point visual analog scale.

Secondary

MeasureTime frame
Complications of shoulder dislocation reduction (fracture, nerve damage, vascular damage). Timepoint: Immediately after dislocation reduction. Method of measurement: Clinical examination, radiography if needed.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbbas Moradi

Hamedan University of Medical Sciences

a.moradi@umsha.ac.ir+98 81 3838 0572

Outcome results

None listed

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