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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03466307
Other study ID # 198
Secondary ID
Status Completed
Phase N/A
First received February 21, 2018
Last updated March 8, 2018
Start date January 1, 2015
Est. completion date October 15, 2017

Study information

Verified date March 2018
Source Suleyman Demirel University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date October 15, 2017
Est. primary completion date July 1, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Ultrasonography
Ultrasonographic examination of shoulder

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Suleyman Demirel University

Outcome

Type Measure Description Time frame Safety issue
Primary Anterior circumflex humeral artery peak systolic velocity Ultrasonographic examination 1 week
Primary Anterior circumflex humeral artery resistive index Ultrasonographic examination 1 week
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