Capillary-Venous Paired Data Collection (NCT05926362) | Clinical Trial Compass
SuspendedNot Applicable
Capillary-Venous Paired Data Collection
Stopped: Paused for interim analysis
United Kingdom800 participantsStarted 2025-02-10
Plain-language summary
Capillary-venous paired data collection.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
CANCER COHORT:
Subjects fulfilling all of the following inclusion criteria are eligible for the study:
* Age ≥18 years old at the time of study entry
* Currently receiving standard-of-care systemic anti-cancer therapy (chemotherapy, immunotherapy, endocrine and targeted therapy) for solid organ malignancy
* Scheduled to be undergoing routine venous laboratory blood tests as part of the standard of care
* Able to provide capillary whole blood donation from pricking three different fingers on one hand
* Can provide written informed consent
* In the Investigator's opinion, is able and willing to comply with all study requirements
The presence of any one of the following exclusion criteria will lead to the exclusion of the subject:
* History or current diagnosis of haematological malignancy (including bone and lymph)
* Inadequate use and understanding of the English language, requiring a translator
HEALTHY COHORT
Subjects fulfilling all of the following inclusion criteria are eligible for the study:
* Age ≥18 years old at the time of study entry
* Can provide written informed consent
* Have an NHS number (to enable ordering and tracking of laboratory FBC tests)
* Registered with a GP
* In the Investigator's opinion, is able and willing to comply with all study requirements
The presence of any one of the following exclusion criteria will lead to the exclusion of the subject:
* Inadequate use and understanding of the English language, requiring a translator
* Been hospital…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Coefficient of Variance of the difference between the lab results and the Liberty results
Timeframe: 3 years
2
Bias (including %bias and absolute bias) between the lab results and the Liberty results
Timeframe: 3 years
3
Regression between the lab results and the Liberty results