Clinical Trials Directory

Trials / Completed

CompletedNCT03466307

Ultrasonographic Parameters and Life Quality in Nocturnal Shoulder Pain

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

Status
Completed
Phase
Study type
Observational
Enrollment
90 (actual)
Sponsor
Suleyman Demirel University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
DEVICEUltrasonographyUltrasonographic examination of shoulder

Timeline

Start date
2015-01-01
Primary completion
2016-07-01
Completion
2017-10-15
First posted
2018-03-15
Last updated
2018-03-15

Source: ClinicalTrials.gov record NCT03466307. Inclusion in this directory is not an endorsement.

Ultrasonographic Parameters and Life Quality in Nocturnal Shoulder Pain (NCT03466307) · Clinical Trials Directory