Endoprosthesis Metal Toxicity Study
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Bone Tumor
- Cancer of Bone
- Chemotherapy Effect
- Cognitive Decline
- Cognitive Impairment
- Heart Diseases
- Memory Problem
- Type
- Observational
- Design
- Observational Model: CohortTime Perspective: Prospective
Participation Requirements
- Age
- Between 18 years and 100 years
- Gender
- Both males and females
Description
At your first visit you will be asked to do the following: Sign the consent document. Patient Interview: An interview will be conducted by the study coordinator on the research team. They will ask your past surgical history, health history, medications, and your cognition. Informant Interview: A clo...
At your first visit you will be asked to do the following: Sign the consent document. Patient Interview: An interview will be conducted by the study coordinator on the research team. They will ask your past surgical history, health history, medications, and your cognition. Informant Interview: A close friend, spouse of relative of you will be interviewed about your day-day cognition. Memory Interview: You will be evaluated on your memory and thinking skills three total times. One to determine baseline, and then repeated at one year and two years. You will answer questions that evaluate various thinking abilities such as concentration, memory, reasoning, and learning. Blood Draw: You will have a blood draw three times (4.2-5 tablespoons) to determine your baseline, 1 year, and 2 year research results. 6: Echocardiogram: You will be asked to have three echocardiograms. One to determine baseline, and then repeated at one year and two years.
Tracking Information
- NCT #
- NCT04755140
- Collaborators
- National Institutes of Health (NIH)
- National Heart, Lung, and Blood Institute (NHLBI)
- National Institute on Aging (NIA)
- Investigators
- Principal Investigator: Matthew Houdek, MD Mayo Clinic