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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03848273
Other study ID # LNMU-FPGE-Neuro-POSTER-1
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 20, 2019
Est. completion date August 31, 2022

Study information

Verified date February 2019
Source Lviv National Medical University
Contact Andriy Kuzminskyy, M.D.
Phone +380973192791
Email a.kuzminskyy@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Improve the effectiveness of treatment and prognosis in patients with cerebrovascular accident by early detection of the risk of developing epileptic seizures.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date August 31, 2022
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- informed consent to participate in the study signed by the patient / relative of the patient / the legal representative of the patient

- age over 18 years

- stroke, confirmed by neuroimaging

- light to moderate stroke (score on National Institutes of Health Stroke Scale).

Exclusion Criteria:

- recanalization therapy

- previous epileptic seizures and history of epilepsy

- psychiatric diseases in history

- previous stroke

- traumatic brain injury

- brain tumors.

- inflammatory and infectious diseases

- decompensated physical illness.

- pregnancy.

Study Design


Locations

Country Name City State
Ukraine Danylo Halytsky Lviv National Medical University Lviv

Sponsors (1)

Lead Sponsor Collaborator
Lviv National Medical University

Country where clinical trial is conducted

Ukraine, 

Outcome

Type Measure Description Time frame Safety issue
Other Death Coroner report will be used to assess this outcome measure. 1 year
Primary First epileptic seizure Patient's dairy will be used to assess this outcome measure. 1 year
Secondary Longest seizure-free period Patient's dairy will be used to assess this outcome measure. 1 year
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