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Night Pain in Patients With Rotator Cuff Syndrome

G

Gaziosmanpasa Research and Education Hospital

Status

Completed

Conditions

Rotator Cuff Tear
Shoulder Pain
Shoulder Tendinitis
Shoulder Impingement Syndrome

Treatments

Other: Night Pain in Patients with Rotator Cuff Syndrome

Study type

Interventional

Funder types

Other

Identifiers

NCT03894761
13.06.18/69

Details and patient eligibility

About

The aim of this study is to determine the factors that may be associated with night pain in patients diagnosed with rotator cuff syndrome by clinical and magnetic resonance imaging.

Full description

Patients who were diagnosed as rotator cuff syndrome by clinical examination and magnetic resonance imaging will be included in this prospective study.

Demographic data (gender, age, education level, occupation), shoulder pain duration, history of trauma to the shoulder, smoking, dominant arm and diabetes will be questioned and body mass indexes will be calculated. Active shoulder range of motion of the patients will be measured by goniometer and recorded .

Specific tests, which are important for rotator cuff lesion, will be performed to determine whether they are positive or not.

Magnetic resonance imaging of the patients with shoulder pathology will be recorded.

A visual analog scale will be used to determine the intensity of day and night pain. Shoulder Shoulder Pain and Disability Index to assess shoulder disability of patients, SF-36 form will be filled by patient to evaluate the effect of shoulder pathology and Kinesiophobia Score to assess the avoidance of pain induced movement.

Enrollment

61 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • To be diagnosed with rototor cuff pathology by magnetic resonance imaging
  • Age range between 18-65 years old
  • To be literate and cooperative

Exclusion criteria

  • Having shoulder pathology other than rototor cuff pathology (Glenohumeral instability, Bisipital tendon lesions, Glenohumeral joint osteoarthritis, Acromioclavicular joint osteoarthritis, Milwaukee shoulder)
  • Having complete rotator cuff tear
  • Patients with a history of shoulder or cervical surgery
  • The presence of cervical pathology
  • Patients with a history of fracture in the shoulder with pain
  • Local corticosteroid injection history for the shoulder (over the last 6 months) and using painkiller regularly
  • Physical therapy history for the shoulder (in the last 3 months)
  • The presence of systemic inflammatory disease
  • Malignancy
  • Pregnancy
  • A history of any psychiatric disorders

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

61 participants in 1 patient group

Patients with Rotator Cuff Syndrome
Other group
Description:
The patients diagnosed with rotator cuff syndrome by clinical and magnetic resonance imaging.
Treatment:
Other: Night Pain in Patients with Rotator Cuff Syndrome

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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