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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06032585
Other study ID # Dnr 2022-06697-01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 8, 2024
Est. completion date October 2025

Study information

Verified date April 2024
Source Region Skane
Contact Markus Stiehm
Phone +4640336379
Email Markus.Stiehm@skane.se
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Popular science summary of the project The purpose of the study is to investigate in a Swedish population how well the investigators' previous ultrasound findings match the final diagnosis (PD, APS or ET) after a particularly long follow-up time, which greatly increases the certainty that the diagnosis does not change more and is thus correct. Furthermore, the investigators want to study whether the initial ultrasound findings have changed during the control interval and whether measurement results regarding the diameter in one of the fluid-filled rooms in the brain (third ventricle) can be correlated with the development of cognitive impairment or dementia later in the course of the disease. For this, this study have got ethical permission to go into the patients' medical records and to call a subgroup back to the clinic to be able to do a new examination and a memory test.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date October 2025
Est. primary completion date October 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Patients with parkinsonism or essential tremor who came into contact with our clinic before 2017 - Satisfactory transcranial bone window - Previous TU (clinical indication) Exclusion Criteria: - No transcranial bone window

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Sweden Skåne Univ Hospital Malmö Skåne

Sponsors (1)

Lead Sponsor Collaborator
Region Skane

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation Is hyperechogenicity of substantia nigra at mesencephal plane (measured bilaterally in mm2 by transcranial b-mode sonography correlated with a high percentage of patients with classical Parkinsons Disease in contrast to atypical parkinsonism patients? over 7-10 yrs
Secondary Correlation Is 3rd ventricle atrophy (measured in mm by b-mode transcranial sonography) correlated with a high % of demented patients in the cohort? 7-10 (retrospective)
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