Ultrasonographic Parameters and Life Quality in Nocturnal Shoulder Pain

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

90 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-01-01

Study Completion Date

2017-10-15

Brief Summary

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This study aimed to investigate the effects of nocturnal pain on clinical and ultrasonographic parameters in patients with rotator cuff tendinopathy.

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Detailed Description

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Thirty patients with nocturnal pain, 30 patients without nocturnal pain, and 30 healthy subjects were included in the study. The demographic characteristics and body mass indexes of the patients were recorded. The visual analogue scale was used to determine pain severity. The American Shoulder and Elbow Surgeons Scale Assessment, Short Form-36 and Beck Depression Inventory were used to determine patients' shoulder function, general quality of life and depression levels, respectively. The peak systolic velocity and resistive index of anterior circumflex humeral artery was assessed with power doppler ultrasonography.The peak systolic velocity and resistive index of anterior circumflex humeral artery values of the affected and unaffected sides were compared.

Conditions

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Musculoskeletal Pain

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Group A

Thirty patients with nocturnal shoulder pain

Ultrasonography

Intervention Type DEVICE

Ultrasonographic examination of shoulder

Group B

Thirty patients without nocturnal shoulder pain

Ultrasonography

Intervention Type DEVICE

Ultrasonographic examination of shoulder

Group C

Healthy controls

Ultrasonography

Intervention Type DEVICE

Ultrasonographic examination of shoulder

Interventions

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Ultrasonography

Ultrasonographic examination of shoulder

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients aged over 18 years diagnosed with rotator cuff tendinopathy

Exclusion Criteria

* Severe limitation and pain in head and neck movements
* Loss of strength
* Sensation and reflexes loss in the upper extremity
* Limitation in passive shoulder movements on physical examination
* Systemic rheumatic disease
* Diabetes mellitus
* Malignant disease
* Active infection
* Intraarticular injection
* Trauma
* Dementia
* History of surgery
* Bilateral should pain
* Psychiatric discomfort
* Smoking history
* Antiinflammatory drugs or received physical therapy within the last 3 months
* Beck depression score of higher than 13.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes