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Completed

NCT Number: NCT03466307

Ultrasonographic Parameters and Life Quality in Nocturnal Shoulder Pain

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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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Ultrasonography

Device

Ultrasonographic examination of shoulder

Primary outcomes

  1. Anterior circumflex humeral artery peak systolic velocity

    Time frame: 1 week

    Ultrasonographic examination

  2. Anterior circumflex humeral artery resistive index

    Time frame: 1 week

    Ultrasonographic examination

Sponsors and collaborators

Lead sponsor

Suleyman Demirel University

Other

Registry information

Official study title

Comparison of Clinical and Ultrasonographic Parameters of Rotator Cuff Tendinopathy Patients With and Without Nocturnal Pain

Important dates

Study start
2015
Primary completion
2016
Study completion
2017
First posted
Mar 15, 2018
Registry last updated
Mar 15, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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