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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05828797
Other study ID # HRU
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 5, 2024
Est. completion date January 1, 2026

Study information

Verified date May 2024
Source Sanliurfa Mehmet Akif Inan Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In our study, we aimed to examine the muscles and tendons of the shoulder region on the plegic side of patients with hemiplegia by elastography and to investigate whether there is a relationship between the course of the disease and the course of the lesions that will occur in the shoulder.


Description:

Patients over the age of 18 who apply to our clinic and have hemiplegia complaints will be evaluated. Patients' age, gender, occupation, habits, disease duration, upper extremity with complaints, dominant upper extremity, additional disease, weight and height values will be recorded. In the physical medicine and rehabilitation department examination of the patients, the patients will be evaluated with the brunnstrom staging used in hemiplegic patients. The elastography of the shoulder on the side with hemiplegia and the elastography of the shoulder on the side without complaints will be examined. Thus, the patient's side with the complaint will be checked by comparing the healthy side.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date January 1, 2026
Est. primary completion date January 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Volunteer patients 2. Patients over 18 years old 3. Patients with hemiplegia 4. Patients without any rheumatic disease 5. Patients without any neurological deficit and muscle disease 6. Not having received ftr treatment to the shoulder area in the last 3 months 7. No injection to the shoulder area in the last 3 months 8. Not having any surgical procedure on the shoulder area 9. Not to be pregnant Exclusion Criteria: 1. Patients with any rheumatic disease 2. Patients with any neurological deficit and muscle disease 3. To have received ftr treatment to the shoulder area in the last 3 months 4. Being under 18 years old 5. Having an infectious disease 6. Having any benign or malignant disease 7. Any surgical procedure to the shoulder area 8. Pregnancy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Harran University Faculty of Medicine, Department of Physical Medicine and Rehabilitation, Sanliurfa Sanliurfa

Sponsors (1)

Lead Sponsor Collaborator
Sanliurfa Mehmet Akif Inan Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of Shoulder Region With Share-Wave Ultrasound Elastography in Patients With Hemiplegia Hemiplegia 02/05/2023-02/05/2024
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