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Risk of Dementia and Heart Failure in Total Joint Arthroplasty
The purpose of this research is to understand whether patients who previously had total hip or total knee replacement experience memory, thinking or heart problems. This study will help us determine if and how often these problems occur.
At your first visit you will be asked to do the following. * Sign this informed consent document. * Questionnaire: You will be asked to complete a questionnaire about your family history of neurological diseases and current and past physical thinking activities. * Interview: The interview will be performed by the study coordinator who is a member of the research team. It will take about 20-30 minutes to complete. You will be asked to answer questions about your general health, surgeries, medications, and your memory and thinking skills. * Memory Interview: You will have an evaluation of your memory and thinking skills. You will answer questions and perform tasks that evaluate various thinking abilities such as concentration, memory, reasoning, and learning. * Blood draw: Have a sample of blood drawn (4.2-5 tablespoons) for clinical and research tests. * Magnetic Resonance Imaging (MRI) of your brain (optional): If you agree to participate, you will be asked to have MR imaging of your brain. * Echocardiogram: You will be asked to have an echocardiogram of your heart. * Follow-up visit in 2-3 years: You will be asked to return to Mayo for your second study visit in 2-3 years. At this visit, you will be asked to complete the same memory and thinking tests described for the first visit. You will also be asked to repeat the echocardiogram.
Age
18 - 100 years
Sex
ALL
Healthy Volunteers
Yes
Mayo Clinic in Rochester
Rochester, Minnesota, United States
Start Date
October 1, 2019
Primary Completion Date
September 27, 2021
Completion Date
September 27, 2021
Last Updated
December 8, 2021
115
ACTUAL participants
Questionnaires
BEHAVIORAL
Interviews
BEHAVIORAL
Blood draw
OTHER
Magnetic Resonance Imaging
RADIATION
Echocardiogram
DIAGNOSTIC_TEST
Lead Sponsor
Mayo Clinic
Collaborators
NCT06346132
NCT07482709
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07351968