- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01885975
Personality Profile of Patients With Apical Ballooning Syndrome
February 13, 2015 updated by: Abhiram Prasad, Mayo Clinic
Personality Profile of Patients With Apical Ballooning Syndrome (ABS)
The investigators' hypothesis is that patients with apical ballooning syndrome (ABS) will manifest a personality profile that differs than that of a population of similar range of ethnic and socioeconomic status.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
53
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Minnesota
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Rochester, Minnesota, United States, 55905
- Mayo Clinic in Rochester
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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
Non-Probability Sample
Study Population
This study will be conducted among participants in the Mayo Clinic Apical Ballooning Registry.
These patients were prospectively diagnosed with Apical Ballooning Syndrome at the time of presentation with their acute illness, and consented to participation in a registry.
They are residents of Olmsted County, and the surrounding regions for which the Mayo Clinic serves as a tertiary care center.
Enrollment in the registry requires satisfaction of standard criteria for the diagnosis of ABS and includes the administration of a standardized questionnaire.
Subjects have agreed to participate in yearly follow up questionnaires about their health status.
Description
Inclusion criteria:
- Patients who have suffered with ABS
- Adults (18 years or older)
- Able to read English at a 6th grade level (questionnaires are self-administered and written in English)
Exclusion criteria:
- Have withdrawn from the registry
- Have died
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Range of personality traits as assessed by the "NEO-PI-3"
Time Frame: Baseline: the traits will be assessed once upon enrollment into the study
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The "NEO PI-3" measures the five major domains of personality, which are:
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Baseline: the traits will be assessed once upon enrollment into the study
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Abhiram Prasad, MD, Mayo Clinic
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
July 1, 2013
Primary Completion (Actual)
September 1, 2014
Study Completion (Actual)
September 1, 2014
Study Registration Dates
First Submitted
June 20, 2013
First Submitted That Met QC Criteria
June 21, 2013
First Posted (Estimate)
June 25, 2013
Study Record Updates
Last Update Posted (Estimate)
February 16, 2015
Last Update Submitted That Met QC Criteria
February 13, 2015
Last Verified
February 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 13-003419
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.
Clinical Trials on Apical Ballooning Syndrome
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Mayo ClinicCompletedApical Ballooning SyndromeUnited States
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Mayo ClinicUnited States Department of DefenseCompletedMyocardial Infarction | Coronary Endothelial Dysfunction | Apical Ballooning SyndromeUnited States
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University of Sao PauloFundação de Amparo à Pesquisa do Estado de São PauloCompleted
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Aga Khan UniversityCompletedChronic Apical PeriodontitisPakistan
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Postgraduate Institute of Dental Sciences RohtakUnknownChronic Apical PeriodontitisIndia
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Monaldi HospitalBambino Gesù Hospital and Research InstituteRecruitingLeft Ventricular Apical Hypoplasia (LVAH), New Rare ConditionItaly
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Academisch Medisch Centrum - Universiteit van Amsterdam...UnknownEffectiveness of Microscope During Apical Surgery in Endodontic Treated Teeth.Netherlands