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Arthroscopic Coracoid Bone Tunnel-Free Anchor Combined with Loop Plate Suspension Technique for Early Clinical Follow-Up Study of Rockwood Type III Acute Acromioclavicular Joint Dislocation

Arthroscopically-assisted Tunnel-less Coracoid EndoButton Combined with Suture Anchors for the Treatment of Rockwood Type ? Acute Acromioclavicular Joint Dislocation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117742
Enrollment
Unknown
Registered
2026-01-28
Start date
2026-01-28
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Acute Rockwood Type ? Acromioclavicular Joint Dislocation

Interventions

Arthroscopic bone-tunnel–free EndoButton–anchor fixation for acute Rockwood type III acromioclavicular joint dislocation group:NA

Sponsors

The Second Affiliated Hospital of Inner Mongolia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Acromioclavicular joint dislocation (Rockwood Type ?) was confirmed by imaging examinations (X-ray/CT). 2. Acute injury: the time interval from injury to surgery was = 3 weeks. 3. The patient underwent the arthroscopically-assisted tunnel-less coracoid suture anchor combined with EndoButton suspension technique in our hospital. 4. Complete preoperative, postoperative and follow-up clinical and imaging data were available. 5. The follow-up duration was = 6 months.

Exclusion criteria

Exclusion criteria: 1. Complicated with severe shoulder fractures (e.g., distal clavicular fractures, scapular/coracoid fractures) requiring alternative fixation methods. 2. A history of previous ipsilateral shoulder surgery or severe shoulder joint diseases (e.g., irreparable severe rotator cuff tears, infection, tumor, etc.). 3. Complicated with brachial plexus/vascular injuries requiring emergency specialized management. 4. Insufficient follow-up duration of less than 6 months or loss of key outcome indicators.

Design outcomes

Primary

MeasureTime frame
Pain level;Constant-Murley;ASES;Range of motion, ROM;

Secondary

MeasureTime frame
coracoclavicular space;complications;

Countries

China

Contacts

Public ContactJie Xu

The Second Affiliated Hospital of Inner Mongolia Medical University

docxujie2024@163.com+86 137 0471 1898

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026