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Amyotrophic Lateral Sclerosis Web Based Patient Care Database: ALSConnection.Org

NCT00302198 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 15000

Last updated 2010-03-02

No results posted yet for this study

Summary

The purpose is to collect data for ALS research. The data will be used to learn more about the origin of ALS and to improve quality of care for people with ALS. The information you provide in the ALS registry will be used to evaluate variations in patient care, adherence to standards of care and also to help foster ALS research.

Conditions

Interventions

BEHAVIORAL

ALS Registry

Sponsors & Collaborators

Principal Investigators

  • Robert G Miller, MD · California Pacific Medical Center

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-31
Primary Completion
2010-02-28
Completion
2010-02-28

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00302198 on ClinicalTrials.gov