- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01956292
Continuous Monitoring of Blood Pressure in Spontaneous Intraparenchimal Cerebral Haemorrhage (BP-MONICH)
October 5, 2013 updated by: Simone Vidale, Azienda Ospedaliera Sant'Anna
Observational Study of Continous Monitoring of Arterial Blood Pressure in Spontaneous Intraparenchimal Cerebral Haemorrhage
Evaluation of blood pressure variability in the acute phase of intraparenchimal cerebral haemorrhage and its consequences to clinical outcome
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Simone Vidale, MD
- Phone Number: 00390315859282
- Email: simone.vidale@hsacomo.org
Study Locations
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Como, Italy, 22100
- AO Sant'Anna Hospital
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Contact:
- Simone Vidale, MD
- Phone Number: 00390315859282
- Email: simone.vidale@hsacomo.org
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients admitted to hospital for intraparenchimal cerebral haemorrhage
Description
Inclusion Criteria:
- hospitalization only for spontaneous intraparenchimal cerebral haemorrhage
- age over 18 years
Exclusion Criteria:
- cerebral haemorrhage secondary to other causes
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Intraparenchimal cerebral haemorrhage
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
evaluation of blood pressure varibility on clinical course in patients with cerebral haemorrhage
Time Frame: Day 7
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Day 7
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2013
Primary Completion (ANTICIPATED)
October 1, 2014
Study Completion (ANTICIPATED)
June 1, 2015
Study Registration Dates
First Submitted
September 29, 2013
First Submitted That Met QC Criteria
October 5, 2013
First Posted (ESTIMATE)
October 8, 2013
Study Record Updates
Last Update Posted (ESTIMATE)
October 8, 2013
Last Update Submitted That Met QC Criteria
October 5, 2013
Last Verified
October 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- OSA-0002
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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