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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01506804
Other study ID # H-4-2010-002
Secondary ID
Status Completed
Phase N/A
First received May 5, 2011
Last updated August 9, 2016
Start date November 2010
Est. completion date April 2016

Study information

Verified date August 2016
Source Frederiksberg University Hospital
Contact n/a
Is FDA regulated No
Health authority The Capital Region of Denmark ':'
Study type Interventional

Clinical Trial Summary

Many patients experience an effect of steroid injection, however the effect is often short lasting and recurrence of symptoms is common. The short term effect of injection has been shown to be much better than exercise therapy; however over time the superior effect of injection compared to exercise does not last. Injection in combination with exercise therapy might be a more sufficient therapy than injection alone. The aim of this study is to investigate a combination of steroid injection and a 10 week exercise program. In addition, the study tests the validity of clinical impingement tests using ultrasound verified impingement as gold standard.


Description:

For many patients unspecific pain and reduced motion in the shoulder is a common complaint. It is believed that the main reason for shoulder pain comes from inflammation of the bursa.

Many patients experience an effect of steroid injection, however the effect is often short lasting and recurrence of symptoms is common. Exercise therapy for the muscles around the shoulder joint is also common treatment for shoulder pain. The short term effect of injection has been shown to be much better than exercise therapy; however over time the superior effect of injection compared to exercise does not last. The anti-inflammatory and pain releasing effect of steroid injection in combination with exercise therapy increasing the strength and control of the muscles around the shoulder joint, might be a more sufficient therapy than injection alone. Thus, the aim of this study is to investigate a combination of steroid injection and a 10 week exercise program in patients with a painful shoulder.

Many different clinical tests are used to examine the pathological compression of the bursa during motion in the shoulder joint (impingement). However, it is actually not known if the pain in motion is caused by compression of the bursa. Part of this study therefore is to test the validity of clinical impingement tests using ultrasound verified impingement as gold standard.

Studies comparing injection given guided by ultrasound to blind injections have shown that the ultrasound guided injections are more likely to place the active stuff correctly in the swollen bursa. In this study all injections will be given ultrasound guided. In the ultrasound examination the thickness of the bursa will be measured in all patients in order to investigate if swollenness of the bursa can explained the pain and dysfunction of the shoulder joint


Recruitment information / eligibility

Status Completed
Enrollment 99
Est. completion date April 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Pain and reduced motion in the shoulder for more than four weeks

- Ultrasound verified swollenness of the bursa.

Exclusion Criteria:

- Bilateral pain in the shoulder joints

- Rupture of the rotator cuff or biceps tendons

- Generalised disease which can explain the shoulder pain

- OA in the shoulder joint

- Diabetes

- Positive compression test of the cervical spine

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
methylprednisolone
Steroid injection X 2 and 10 weeks exercise program of painful shoulder vs exercise program of contralateral shoulder

Locations

Country Name City State
Denmark The Parker Institute, Frederiksberg Hospital Frederiksberg

Sponsors (5)

Lead Sponsor Collaborator
Frederiksberg University Hospital Aase and Ejnar Danielsens Foundation, Fund for Physiotherapy in Private Practice, Oak Foundation, The Danish Physiotherapy Foundation

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain in the shoulder in both rest and motion (VAS) 6 months No
Secondary Ultrasound 6 months No
Secondary Strength 6 months No
Secondary Clinical impingement 6 months No
Secondary Shoulder function 6 months No
See also
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Recruiting NCT06220643 - Steroid Injection With Exercise for Subacromial Bursitis N/A
Active, not recruiting NCT03752619 - Peripheral Nerve Stimulation(PNS) for Subacromial Impingement Syndrome(SIS) N/A
Not yet recruiting NCT06435494 - Cross-sectorial Use of Patient-Reported Outcomes in Chronic Degenerative Shoulder Conditions N/A
Recruiting NCT04146987 - Cost-Effectiveness of Rotator Cuff Repair Methods N/A
Completed NCT01702233 - TRARO (Traumeel® S in Rotator Cuff Syndrome)-Study Phase 3
Recruiting NCT06384430 - Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters