Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04137315
Other study ID # IRAS: 272300
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 14, 2020
Est. completion date January 29, 2021

Study information

Verified date February 2021
Source Entia Ltd
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a data collection study to compare diagnostic methods of a prototype of a home monitoring device against laboratory testing in the hospital.


Description:

The device/monitoring system being developed measures the haemoglobin and haematocrit levels in blood from a single drop of blood. By measuring these blood parameters, participants are able to monitor their haemoglobin level at home. The use of the device will take place in the participant's home to simulate what the investigators believe will be the ideal location for people who would prefer to self-manage their condition. This study is a data collection study to evaluate the performance of the prototype.


Recruitment information / eligibility

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.

Study Design


Intervention

Device:
Blood measurement
Single fingerprick to measure haemoglobin and haematocrit measurements using a potential haemoglobin home monitoring system.

Locations

Country Name City State
United Kingdom Hull University Teaching Hospitals NHS Trust Hull

Sponsors (1)

Lead Sponsor Collaborator
Entia Ltd

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quantitative capture of measurement system Data collection for evaluation of measurement system 6 months
See also
  Status Clinical Trial Phase
Recruiting NCT06386172 - Electronic Decision-support System to Improve Detection and Care of Patients With Chronic Kidney Disease in Stockholm N/A
Recruiting NCT04910867 - APOL1 Genetic Testing Program for Living Donors N/A
Completed NCT03434145 - Changes of Ocular Structures After Hemodialysis in Patients With Chronic Kidney Diseases N/A
Recruiting NCT04984226 - Sodium Bicarbonate and Mitochondrial Energetics in Persons With CKD Phase 2
Active, not recruiting NCT05887817 - Effects of Finerenone on Vascular Stiffness and Cardiorenal Biomarkers in T2D and CKD (FIVE-STAR) Phase 4
Recruiting NCT05318196 - Molecular Prediction of Development, Progression or Complications of Kidney, Immune or Transplantation-related Diseases
Terminated NCT05022329 - COVID-19 Vaccine Boosters in Patients With CKD Phase 2/Phase 3
Not yet recruiting NCT04925661 - HEC53856 Phase Ib Study in Patients With Non-dialysis Renal Anemia Phase 1
Recruiting NCT04961164 - Resistant Starch Prebiotic Effects in Chronic Kidney Disease N/A
Completed NCT05015647 - Low Protein Diet in CKD Patients at Risk of Malnutrition N/A
Completed NCT03426787 - Helping Empower Liver and Kidney Patients N/A
Recruiting NCT06094231 - Treating Patients With Renal Impairment and Altered Glucose MetAbolism With TherapeutIc Carbohydrate Restriction and Sglt2-Inhibiton - a Pilot Study N/A
Completed NCT04363554 - The Kidneys Ability to Concentrate and Dilute Urine in Patients With Autosomal Dominant Polycystic Kidney Disease N/A
Recruiting NCT04831021 - Pre- or Per-dialytic Physical Exercise : a Cardioprotective Role? N/A
Terminated NCT04877847 - Multi-Center Trial Utilizing Low Frequency Ultrasound in the Prevention of Post-Contrast Acute Kidney Injury N/A
Recruiting NCT04422652 - Combination of Novel Therapies for CKD Comorbid Depression Phase 2
Completed NCT05055362 - Effect a Honey, Spice-blended Baked Good Has on Salivary Inflammation Markers in Adults: a Pilot Study N/A
Not yet recruiting NCT06330480 - Check@Home: General Population Screening for Early Detection of Atrial Fibrillation and Chronic Kidney Disease N/A
Recruiting NCT03176862 - Left Ventricular Fibrosis in Chronic Kidney Disease N/A
Terminated NCT02539680 - Intestinal Phosphate Transporter Expression in CKD Patients N/A