Affinity: Hospital Trial

NCT04211727 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 247

Last updated 2022-03-29

No results posted yet for this study

Summary

Method comparison study to compare the Affinity prototype device using a capillary blood sample against routine venous laboratory results, in patients undergoing systemic anti-cancer therapy (SACT). Tests will be performed by healthcare professionals (Cohort 1) and participants self-testing (Cohort 2)

Conditions

Interventions

DIAGNOSTIC_TEST

Capillary finger prick blood sample

Patients will have a blood finger prick sample

Sponsors & Collaborators

  • The Christie NHS Foundation Trust

    collaborator OTHER
  • Entia Ltd

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-10-26
Primary Completion
2022-01-17
Completion
2022-01-17

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04211727 on ClinicalTrials.gov