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CKD Registry

Chronic Kidney Disease Research Registry

medical-cross
Chronic kidney disease
user
All genders
person-wave 18-100
world
Recruiting now

Overview

Principal Investigator: Lesley Inker

Patients with Chronic Kidney Disease(CKD) who receive medical care at Tufts Medicine will be invited to join a CKD research registry. The registry will record their medical information related to CKD and future researchers will be allowed to contact patients to ask if they would like to join a CKD related research study. There is nothing patients have to do once they join the registry, and joining a CKD research study is entirely optional.

Study details

Inclusion Criteria
  • Patients with CKD who receive medical care at Tufts medicine.
Exclusion Criteria
  • - Patients on dialysis.
  • Non-Native English speakers other than those who speak Spanish or Mandarin.
  • - Cognitively impaired adults (adults with impaired-decision making capacity) without a parent or guardian to consent for them.
Study Requirements

There are no medications, procedures, or any interventions as part of the CKD Research Registry. If you are receiving or seeking care at Tufts Medical Center or MelroseWakefield Healthcare, you will be asked if you wish to be included in the CKD Research Registry for an indefinite period of time. If you agree to be included in the CKD Research Registry you are giving permission to be contacted to be invited to participate in future CKD research studies. Your CKD related health information will be recorded and stored in a safeguarded database.

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