TightRope AcromioClavicular Study; TRACS.

´Operative TightRope stabilisation versus conservative treatment of Rockwood III acromioclavicular luxations.'

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON23177

Enrollment

Registered

2009-04-28

Start date

2009-07-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Acromioclavicular luxation, TightRope, shoulder instability

Interventions

1. Operative treatment with artroscopic TightRope system

2. Conservative treatment with slinge and physiotherapy.

Eligibility

Inclusion criteria

Inclusion criteria: 1. AC-dislocation Rockwood type 3 confirmed with CT scan; 2. Presentation within 6 weeks after trauma; 3. Patients older than 18 years; 4. Patients with signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Age younger than 18 years; 2. Glenohumeral instability; 3. Other fractures to the shoulder joint; 4. Frozen shoulder; 5. Earlier attempt to fixate AC; 6. Non compliance.

Design outcomes

Primary

Measure	Time frame
DASH score 6 months and 1 year.	—

Secondary

Measure	Time frame
1. VAS painscore; 2. NSST; 3. Constant Murley score.	—

Contacts

Public ContactB.J.W. Thomassen

Haaglanden Medical Center PO Box 432

b.thomassen@mchaaglanden.nl+31 (0)70 3303109

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)