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Clinical controlled trial of early surgical and non-surgical intervention for chronic pain of long head of the biceps tendon with pulley unstable

Clinical controlled trial of early surgical and non-surgical intervention for chronic pain of long head of the biceps tendon with pulley unstable

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023454
Enrollment
Unknown
Registered
2019-05-28
Start date
2019-06-15
Completion date
Unknown
Last updated
2019-06-03

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

Conditions

Injury of long head of the biceps tendon in shoulder joint

Interventions

A:Conservative treatment
B:Surgical treatment

Sponsors

Shanghai Tenth People’s Hospital, Affiliated to Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? Preoperative physical Examination supports the diagnosis of long head of the biceps tendonitis, such as obvious tenderness, positive Speed test, positive Yergason test and positive DeAnquin test in the projection area of the gap surface between humerus nodules; ? Clear Diagnostics of long head of the biceps tendonitis by X-ray, CT and MRI before operation. Exclude rotator cuff injury, shoulder instability, Bankart injury, SLAP injury and other shoulder diseases; ? Before operation by oral non-steroidal drug treatment, physiotherapy and other conservative treatment for 6 months, clinical symptoms did not significantly improve; ? Through arthroscopic further confirmed that the tendon sheath congestion, edema, long head of the biceps tendon inflammation, Degeneration, and is not accompanied by other shoulder diseases.

Exclusion criteria

Exclusion criteria: ? Suffering from any upper limb neurological disease or a history of neurological disorders of the upper limb; ? Cervical spondylosis; ? Previously had surgery that had an effect on shoulder joint function; ? Patients with mental disorders;? Patients are reluctant to undergo follow-up as planned.

Design outcomes

Primary

MeasureTime frame
pain;muscle strength;function;satisfaction;range of motion;

Countries

China

Contacts

Public ContactKun Tao

Shanghai Tenth People’s Hospital, Affiliated to Tongji University

doctk@163.com+86 13681930606

Outcome results

None listed

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