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NCT00001367 Clinical Trial

Diagnosis and History Study of Patients With Different Neurological Conditions

Healthy Volunteer Clinical Trial

Official title:
Diagnosis and Natural History Protocol for Patients With Different Neurological Conditions

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00001367
Other study ID # 930202
Secondary ID 93-N-0202
Status Recruiting
Phase
First received
Last updated
Start date September 30, 1993

Study information
Verified date February 7, 2024
Source National Institutes of Health Clinical Center (CC)
Contact Vivian S Koo
Phone (301) 435-8518
Email vivian.koo@nih.gov
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This protocol is a screening and natural history protocol, which allows for evaluation of patients and families where neurological conditions are present for enrollment into other studies and will also be used to screen healthy volunteers to create a pool of potential future HV matches for HMCS protocols. Through diagnostic evaluations, data will be collected for research use in this study.

Description:

This protocol is a screening and natural history protocol, which allows for evaluation of patients and families where neurological conditions are present for enrollment into other studies and will also be used to screen healthy volunteers to create a pool of potential future HV matches for HMCS protocols. Through diagnostic evaluations, data will be collected for research use in this study.

Recruitment information / eligibility
Status Recruiting
Enrollment 4100
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 2 Years and older
Eligibility - INCLUSION CRITERIA: - Patients with neurological disorders and subjects with a family history of neurological conditions OR - Healthy volunteers: People age 18 or older who are generally in good health. EXCLUSION CRITERIA: - Patients <2 years old. - Employees of HMCS in NINDS.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States National Institutes of Health Clinical Center Bethesda Maryland

Sponsors (1)
Lead Sponsor Collaborator
National Institute of Neurological Disorders and Stroke (NINDS)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary to screen patients with neurological conditions and family members of patients with neurological conditions for enrollment in additional research protocols The goal is to screen patients with neurological conditions and family members of patients with neurological conditions for enrollment in additional research protocols. No investigational treatments will be administered on this protocol and the NIH physicians will be playing a consultative role to the patient s primary physician. ongoing
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