- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02567162
Multinational Survey of Epidemiology, Morbidity, and Outcomes in Intracerebral Hemorrhage (MNEMONICH)
Multinational Survey of Epidemiology, Morbidity, and Outcomes in Intracerebral Hemorrhage (MNEMONICH)
Study Overview
Status
Conditions
Detailed Description
MNEMONICH is a disease-specific registry of prospectively collected data obtained from the integration and harmonization of preexisting single-center data sets. It was formed to provide clinician-scientists around the world a comprehensive database to direct future studies toward better understanding of ICH. MNEMONICH will help examine global variability in the prevalence of ICH and identify research priorities.
New data for MNEMONICH will be prospectively collected on a wide range of features including demographics, medical history, dates and times of symptom onset, presentation symptoms, hemodynamic signs, initial and chronic medical therapy, diagnostic imaging, laboratory and genetic analyses, pathological data, and surgical and medical management. Future research will be based upon ad hoc analysis of this data.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Diagnosis of spontaneous intracerebral hemorrhage (ICH) met by clinical and imaging criteria
- Age 18 and above
- Able to consent
Exclusion Criteria:
- ICH due to trauma
- ICH due to vascular malformation or aneurysm
- ICH due to brain tumor
- ICH due to underlying infectious lesion (e.g., abscess)
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Modified Rankin Scale score
Time Frame: 90 days
|
90 days
|
Collaborators and Investigators
Collaborators
Investigators
- Study Director: Mario Di Napoli, MD, Centre for Cardiovascular Medicine and Cerebrovascular Disease Prevention
- Principal Investigator: Mahmoud R Azarpazhooh, MD, Western University, Canada
- Principal Investigator: Luca Masotti, MD, Arcispedale Santa Maria Nuova-IRCCS
- Principal Investigator: Adrian R Parry-Jones, MBChB, PhD, University of Manchester and the Salford Royal NHS Foundation Trust
- Principal Investigator: Aurel Popa-Wagner, MD, PhD, University of Rostock
- Principal Investigator: Mark A Slevin, PhD, Manchester Metropolitan University
- Principal Investigator: Craig J Smith, MBChB, MD, University of Manchester and the Salford Royal NHS Foundation Trust
- Principal Investigator: Daniel A Godoy, MD, Hospital Interzonal de Agudos San Juan Bautista
- Principal Investigator: Floris H Schreuder, MD, Maastricht University Medical Center
- Principal Investigator: Michael W Hoffmann, MBChB, PhD, University of Central Florida
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HSC20150655H
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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