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“De invloed van cryotherapie op het postoperatief herstel na een schouderoperatie voor het subacromiaal pijnsyndroom.”

Cryotherapy in the recovery of bursectomy for subacromial pain syndrome.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON25969
Enrollment
70
Registered
2017-04-20
Start date
2017-04-20
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

Postoperative pain and shoulder function after bursectomy for subacromial pain syndrome.

Interventions

35 patients (intervention group) will be allocated to computer-assisted cryotherapy (Zamar® ZTCube) for 2 to 8 weeks after surgery. 35 patients (control group) will be allocated to receive usual care

Sponsors

C.P.J. Visser (CV), M.D., PhD Orthopaedic Surgeon Alrijne hospital Department of Orthopedics
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: SAPS is defined according to the recommendations published in the guidelines for the diagnosis and treatment of SAPS of the Dutch orthopaedic association7. Emphasis is put on a combination of tests to demonstrate SAPS7, 25. The following inclusion criteria are applied: - Pain localized in the deltoid region - Complaints for more than 6 months - Unsuccessful physical therapy for at least six weeks - Exacerbation of pain when raising the arm - A positive Neer impingement sign, and an only temporarily effect of ultrasound guided subacromial infiltration (lidocain + corticosteroids). - A positive Hawkins-Kennedy test - A painful arc - Scheduled for arthroscopic bursectomy

Exclusion criteria

Exclusion criteria: - No informed consent is obtained - Language barrier - Age <25 years - Full-thickness rotator cuff tear - Restriction of passive shoulder motion (i.e. frozen shoulder). - Glenohumeral osteoarthritis - Calcifying tendonitis - History of a neurological disorder (e.g. stroke, Parkinson, dementia) - Rheumatoid arthritis - Concomitant biceps tenodesis. - Subacromial decompression (Those patients are treated with a pain-buster). - Clinical signs of cervical radiculopathy.

Design outcomes

Primary

MeasureTime frame
The primary study outcome is quality of life reported on the Western Ontario Rotator Cuff index 8 weeks after surgery.

Secondary

MeasureTime frame
Secondary outcomes are VAS for pain in rest, VAS when elevating the arm, Simple Shoulder test, Constant Score, range of motion, use of painkillers and return to work. Additionally, we will daily record pain and use of painkillers until approximately 8 weeks after surgery.

Contacts

Public ContactC.P.J. Visser

Houtlaan 55

cpjvisser@alrijne.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)