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Dutch Arthoscopy Association Rotator Cuff Study

Dutch Arthoscopy Association Rotator Cuff Study - NRC-Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON35617
Enrollment
140
Registered
2007-11-28
Start date
2008-02-04
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

cuff rupture

Interventions

Conventional open and arthroscopic rotator cuff surgery.

Sponsors

Sint Antonius Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: * Full thickness cuff rupture proven on MR-arthrography * Signed Informed Consent form

Exclusion criteria

Exclusion criteria: * age 75 year * neurologic etiology * glenohumeral instability * traumatic shoulder/old fracture * frozen shoulder * reumatoïd arthritis * history of shoulder infection * history of (attempt) cuff repair * history of wound healing problems (dehiscence, infections e.g.) * acromionresection * cuff arthropathy * perioperativally not able to close defect or partial thickness rupture * non compliance with regard to follow up * not capable of speaking and writting dutch language

Design outcomes

Primary

MeasureTime frame
Disabilities of Arm, Shoulder and Hand Score (DASH) at different follow up visits (pre-op; 6 wk; 3 mth; 6 mth; 12 mth; 24 mth). Addendum: Standardized RoM*s before and after surgery

Secondary

MeasureTime frame
Visual Analogue Scale for pain (VAS pain), Simple Shoulder Test (SST), Constant Murley score and clinical shoulder function 12 months post operativally. Evauation of cuff quality by MR-arthrography 12 months post operativally. Addendum: EMG shoulder muscle activation patterns during standardized tasks --> Activation ratio

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)