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United Kingdom Rotator Cuff Trial

Clinical effectiveness and cost-effectiveness of open and arthroscopic rotator cuff repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN97804283
Enrollment
270
Registered
2007-06-29
Start date
2007-07-01
Completion date
Unknown
Last updated
2018-01-08

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

Conditions

Musculoskeletal Diseases Musculoskeletal Diseases Shoulder lesions

Interventions

Current information as of 21/10/10: Each participant will be randomised to one of the following arms: Arm 1 - Open/mini-open surgery Arm 2 - Arthroscopic surgery Initial information at time of regi

Sponsors

University of Oxford (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 50 years or older 2. Suffer from degenerative rotator cuff tear 3. Have full thickness rotator cuff tear 4. Tear diagnosed using Magnetic Resonance Imaging (MRI) or ultrasound scan 5. Patient able to consent

Exclusion criteria

Exclusion criteria: 1. Previous surgery on affected shoulder 2. Dual shoulder pathology 3. Significant problems in other shoulder 4. Rheumatoid arthritis / systemic disease 5. Significant osteoarthritis problems 6. Significant neck problems 7. Cognitive impairment or language issues

Design outcomes

Primary

MeasureTime frame
The UKUFF Questionnaire at 24 months after entry into study.

Secondary

MeasureTime frame
Resource use measures including use and cost of health services.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 17, 2026