Chronic Kidney Diseases Clinical Trial
Official title:
Project Aura: Data Collection for a Home Monitoring Solution for Patients With Anaemia to Evaluate Delivery of Treatment
Verified date | February 2021 |
Source | Entia Ltd |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This is a data collection study to compare diagnostic methods of a prototype of a home monitoring device against laboratory testing in the hospital.
Status | Completed |
Enrollment | 10 |
Est. completion date | January 29, 2021 |
Est. primary completion date | January 29, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age = 18 years of age. - Adequate english to participate in training sessions and use the analyser. - Patients of the study site who are currently undergoing treatment for anaemia of CKD with ESAs. - Patients who are not pregnant. - Patients who do not have a bleeding disorder. - Patients willing to perform self-tests 2-3 times a week. - Patients capable of providing informed consent before attending training. - Patients or patients with a carer capable of fine manipulation of the device and its consumables. - Patients or patients with a carer who own a smartphone which can download the app related to this study. - Patients or patients with carers who do not have eyesight limitations to be able to read the instructions on the screen of the prototype device. - Patients who are not expected to have to start dialysis treatment during the course of this study. Exclusion Criteria: - Does not have adequate English to participate in training or use the analyser without an interpreter. - Patients of the study site who are not currently undergoing anaemia treatment with ESAs. - Patients of the study site not willing to perform self-tests 2-3 times a week. - Patients of the study site not capable of providing consent or have a suitable, legally acceptable representative present to provide consent before the trial. - Patients who are pregnant. - Patients with a bleeding disorder. - Patients or their nominated carers who are not capable of fine manipulation of the device and its consumables. - Neither patients or their nominated carers do not own a smartphone which can install the app related to this study. - Patients or their nominated carers with eyesight limitations to not be able to read the instructions on the screen of the prototype device. - Patients who are expected to start dialysis treatment during the study. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Hull University Teaching Hospitals NHS Trust | Hull |
Lead Sponsor | Collaborator |
---|---|
Entia Ltd |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Quantitative capture of measurement system | Data collection for evaluation of measurement system | 6 months |
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