Study Details
A Medtronic Product Follow-up Registry
(IRB#: IRB_00184960)
This study will collect information into a follow-up registry from people who have used or intend to use a Medtronic Product. The information collected will be to continue Medtronic product safety and effectiveness and understand the range of product usage in clinical environments such as hospitals. This will help guide development and improvement of medical devices and therapies for patients that inform clinical research. People in the study will provide health information. This includes medical records, interviews, phone calls, mail, emails from the participant, family members, and/or doctors or other health providers. Participants will attend all regularly scheduled doctor visits, tell doctors about medical history, and report any health events such as injuries or hospitalizations. There is no registry end date.
- All genders
- Over 18 years old
- Volunteers with special conditions
- In Person
- Unpaid
Who can participate?
Gender: All genders
Age: Over 18 years old
Volunteers: Volunteers with special conditions
Location: In Person
Inclusion Criteria
- A participant or legally authorized representative (LAR) who can provide authorization and/or consent
- A participant who has been or intends to be treated with an eligible Medtronic product
Exclusion Criteria
- Unable to be contacted for follow-up
- Are currently in another study for a drug or device that may interfere with the study results
Will I be paid for my time?
No
IRB#: IRB_00184960
PI: ALLISON GLINKA PRZYBYSZ
Department: Physical Medicine and Rehabilitation
Approval Date: 2025-02-19 23:02:00
Study Categories: Bone and Muscle Studies
Specialties: Physical Medicine & Rehabilitation
I am Interested