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Completed

NCT Number: NCT00998868

Rotator Cuff Tears in Hemiplegic Shoulder

The purpose of the study is to evaluate the prevalence of rotator cuff tears in the shoulders of hemiplegic patients of different severity.

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Key information

Age range

20 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Seoul National University Hospital

Seoul, South Korea

About this study

Rotator cuff tears are often suspected to contribute hemiplegic shoulder pain. However, it is controversial whether their incidence increases in hemiplegia. Based on the postulate that muscle weakness in hemiplegia predisposes rotator cuff injury due to biomechanical failure, this study aims to investigate whether the rotator cuff tears are associated with the muscle strength of the shoulder by observing hemiplegic shoulders of varying degree of paresis.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • hemiplegia; unilateral weakness of sudden onset
  • secondary to strokes or other brain lesions
  • compatible with brain lesions confirmed by imaging studies

Exclusion criteria

  • bilateral weakness
  • any history of intensive trauma of the shoulder, reported
  • preexisting musculoskeletal disorder of the shoulder

Treatment and study plan

Primary outcomes

  1. Rotator Cuff Tear of the Hemiplegic Shoulder, Confirmed by Ultrasonography

    Time frame: within one month after enrollment

    All patients underwent ultrasonography (USG) for the both, affected and unaffected, shoulders. USG routinely examined biceps, subscapularis, supraspinatus, and infraspinatus tendons as for the partial or complete tears, calcifications, bony irregularity and bursal swellings.

Secondary outcomes

  1. Rotator Cuff Tear of the Unaffected Shoulder, Confirmed by Ultrasonography

    Time frame: within one month after enrollment

    All patients were performed ultrasonography (USG) for the both, affected and unaffected, shoulders. USG routinely examined biceps, subscapularis, supraspinatus, and infraspinatus tendons as for the partial or complete tears, calcifications, bony irregularity and bursal swellings.

  2. Subluxation of the Glenohumeral Joint, Confirmed by Physical Examination

    Time frame: within one month after enrollment

    The glenohumeral joint subluxation was examined by palpating the subacromial regions of the both sides and comparing the affected side with the unaffected side while patients are seated and relaxed. If the palpated space between the acromion and the humeral head was wider on the affected side by one half finger breath or more, it was judged to be subluxation.

  3. Muscle Strength, Measured by Physical Examination, Per Medical Research Council Muscle Strength Grading System

    Time frame: within one month after enrollment

    Muscle strength was measured for forward flexion and abduction of the shoulder per Medical Research Council (MRC) scale in each participants. Their mean +/- SD were calculated in each group.

    MRC scale:

    Grade 5: Normal and can move against full resistance. Grade 4: Reduced but can move against resistance. Grade 3: Can move only against gravity Grade 2: Can move without gravity Grade 1: Only a trace of movement Grade 0: No movement.

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Registry information

Official study title

Observational Study to Evaluate the Prevalence of Rotator Cuff Tears in Hemiplegic Shoulders

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Oct 21, 2009
Registry last updated
Sep 30, 2011

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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