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Comparison of Two Types of Braces in the Treatment of Rockwood Type III AC-dislocations

Conservative Treatment of Rockwood Type III Acromioclavicular Dislocation With Two Different Types of Braces: a Comparative Prospective Randomized Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03261778
Enrollment
35
Registered
2017-08-25
Start date
2017-09-01
Completion date
2021-01-12
Last updated
2021-01-13

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

Conditions

Acromioclavicular Joint Dislocation

Brief summary

In a randomised prospective comparative Trial the investigators aim to compare the conservative Treatment of acromioclavicular dislocations (Rockwood III) with a conventional sling versus a Acromion 2.0 brace, which exerts a direct Reposition force on the Joint. The sling/brace will be worn for 6 weeks and the patients will be regularly checked clinically and radiologically.The investigators are interested in differences of shoulder function, Patient satisfaction as well as cosmetic and radiological results.

Interventions

DEVICEAcromion 2.0 Brace

Acromion 2.0 Brace will be worn for 6 weeks instead of the conventional Mitella sling

Sponsors

University Hospital, Basel, Switzerland
CollaboratorOTHER
Bürgerspital Solothurn
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
Yes

Inclusion criteria

* First acute acromioclavicular dislocation Rockwood Type III

Exclusion criteria

* Previous injury to acromioclavicular Joint * Previous surgery of acromioclavicular Joint * Known hypersensitivity or allergy to fabric of investigational product * Pregnancy * Known or suspected non-compliance, drug or alcohol abuse * Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant

Design outcomes

Primary

MeasureTime frameDescription
Shoulder functionat 6 weeksConstant-Score

Secondary

MeasureTime frameDescription
Degree of lateral clavicle dislocationat initial presentationCoracoclavicular distance on Panorama view in comparison to healthy side

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026