A Study To Evaluate At-Home Monitoring Of Patients With Decompensated Cirrhosis
Overview
Tab Title Description
Study type
ObservationalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 21-005002
About this study
The purpose of this study is to determine if there is a correlation between patient quality of life and rate of hospital readmission in patients hospitalized with decompensated cirrhosis. The REMODI program has already been implemented in the department of medicine at Mayo to monitor subjects via mobile devices after discharge from the hospital. We aim to determine the impact of these interventions.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
Subjects over the age of 18 years.
Ability to provide written, informed consent.
Hospitalized with complications of decompensated cirrhosis.
Exclusion Criteria:
Subjects under 18 years of age.
Subject has uncontrolled mental illness and/or drug or alcohol abuse.
Resides in (or is discharging to) a long-term care facility.
Subject is being actively followed by dialysis or transplant services.
Subject is pregnant.
Subject is being actively treated for cancer.
Subject is identified as end of life by provider.
Subject has dementia, cognitive impairment, or physical condition that limits ability to use home remote monitoring equipment independently, or interact with remote patient monitoring staff (unless a caregiver commits to assisting daily).
Note: Other protocol defined Inclusion/Exclusion Criteria may apply.
Eligibility last updated 05/07/2021. Questions regarding updates should be directed to the study team contact.
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
| Mayo Clinic Location |
Status |
|
Rochester, Minn.
Mayo Clinic principal investigator Douglas Simonetto, M.D. |
Closed for enrollment |
|
More information
Publications
Publications are currently not available