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Elastography in Patients With Hemiplegia

Sponsor
Sanliurfa Mehmet Akif Inan Education and Research Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05828797
Collaborator
(none)
30
Enrollment
20.8
Anticipated Duration (Months)

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

    Detailed 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.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    30 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Evaluation of Shoulder Region With Share-Wave Ultrasound Elastography in Patients With Hemiplegia
    Anticipated Study Start Date :
    May 2, 2023
    Anticipated Primary Completion Date :
    May 2, 2024
    Anticipated Study Completion Date :
    Jan 23, 2025

    Arms and Interventions

    Arm Intervention/Treatment
    Shoulder elastography on the hemiplegic side of patients

    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.
    Shoulder elastography on the non-hemiplegia side of patients

    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.

    Outcome Measures

    Primary Outcome Measures

    1. Evaluation of Shoulder Region With Share-Wave Ultrasound Elastography in Patients With Hemiplegia [02/05/2023-02/05/2024]

      Hemiplegia

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Sanliurfa Mehmet Akif Inan Education and Research Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Veysel Delen, MD, MD, Harran University
    ClinicalTrials.gov Identifier:
    NCT05828797
    Other Study ID Numbers:
    • HRU
    First Posted:
    Apr 25, 2023
    Last Update Posted:
    Apr 25, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:
    Hemiplegia

    Study Results

    No Results Posted as of Apr 25, 2023