ClinicalTrials.gg
SuspendedNCT06445205Updated Apr 8, 2025

Utilising Volumetric Absorptive Microsampling (VAMS) Technology to Monitor Tacrolimus and Creatinine

An observational study in Kidney Transplant Rejection and Kidney Replacement, sponsored by Lancashire Teaching Hospitals NHS Foundation Trust. Suspended at 1 site in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-04-08.

Sponsored by Lancashire Teaching Hospitals NHS Foundation Trust · Observational

Why this study was suspended
Chief Investigator not available
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

Tacrolimus is a medicine given to try and stop rejection of a new kidney after transplant surgery. If too much taken the kidney may be damaged. If not enough taken, the risk of rejection is increased. Creatinine is a waste product made by the muscles and is normally removed from the body by the kidneys. If kidney function gets worse, the creatinine level in the blood goes up and means the new new kidney is not working properly. It is important to monitor levels of tacrolimus and creatinine regularly, to keep the kidney as healthy as possible. Regular monitoring also aids with balancing the amount of tacrolimus that patients need to take.

The COVID-19 pandemic led to changes in the delivery of transplant services. One such changes was a move to the use of point-of-care, and at home devices.

The study involves the set-up a new method in an NHS laboratory to test tacrolimus and creatinine levels in blood collected in the normal blood tubes and to compare the results with this new collection device, to see if the results are the same.

If the results match, patients will continue to collect a blood sample using the new devices and send it to the laboratory. This will save both patients and the NHS time and money as they will not have to travel to a hospital to have their bloods taken.

Read the detailed description

A minimum of 50 adult renal transplant patients (>18 years old) taking tacrolimus as an immunosuppressant will be recruited when attending their routine outpatient follow up appointment, or if selected as eligible by the Renal Consultants and transplant nurses. Written consent will be obtained from all participants.

Patients attending blood clinic to have their routine blood samples taken will also have a finger prick and a small amount of blood (10µl) will be collected by volumetric absorptive micro sampling (VAMS) using the Mitra® device (Neoteryx), according to manufacturer's instructions. Two venous blood samples will be collected from the patients by venepuncture by trained phlebotomists/nurses. A 4ml EDTA and a 4ml serum gel sample (to measure tacrolimus and renal function as part of routine care). Tacrolimus and creatinine are measured in venous blood samples as part of routine patient care therefore these will be processed as normal, and results reported. The paired capillary samples collected using the Mitra® device will be batched and run when appropriate by liquid chromatography-mass spectrometry (LC-MS/MS). Mitra® devices will be stored at -20 degree Celsius, prior to analysis.

Venous EDTA whole blood samples (collected by venepuncture) and capillary whole blood samples (collected by VAMS®) will be analysed for tacrolimus using a validated LC-MS/MS assay in routine clinical use in the lab using the Waters ACQUITY UPLC system and Xevo TQD MS. Capillary whole blood samples (collected by VAMS®) and serum samples will be analysed for creatinine using an LC-MS/MS method which will be developed in house. For the method comparison, serum samples (collected by venepuncture) will be analysed for creatinine using an enzymatic method on the Roche platform. All sample analysis will be performed in an ISO 15189 accredited laboratory.

02

Conditions studied

  • Kidney Transplant Rejection
  • Kidney Replacement
03

In context

Lead sponsor

Lancashire Teaching Hospitals NHS Foundation Trust is the lead sponsor of 10 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult renal transplant patients (>18 years old) taking tacrolimus as an immunosuppressant

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Post renal transplant patients taking tacrolimus
  • having regular bloods taken for tacrolimus and renal function testing.
  • Patients must be taking tacrolimus as part of their regimen.
  • They must be over 18 years of age

Exclusion criteria

Exclusion Criteria:

  • Patients under the age of 18 (the study is for adults only).
  • Vulnerable adults who are deemed unable to give consent themselves - If applicable, this can be assessed using the Trust clinical tool 'Assessment of Mental Capacity'.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
50 participants (estimated)
Patient registry
No

Groups and cohorts

  • Sample collection

    Sample collection via standard phlebotomy as well as point-or-care Mitra device.

    Diagnostic Test: Mitra® device with VAMS® (volumetric absorptive microsampling) technology

Interventions

  • Diagnostic testMitra® device with VAMS® (volumetric absorptive microsampling) technology

    Capillary blood sample

06

What researchers measure

Primary outcomes

  1. Tacrolimus in Capillary Blood Samples

    That Tacrolimus is within range: 10-20ng/ml

    Time frame: 6 months

  2. Creatinine in Capillary Blood Samples

    That Creatinine is within range: 52.2 - 119.3 micromoles/L

    Time frame: 6 months

Secondary outcomes

  1. Tacrolimus is concordant with venous blood sample

    Results match standard venous results for Tacrolimus and is within range:10-20ng/ml then use of VAMS will be implemented into routine clinical practice for monitoring renal patients post transplant.

    Time frame: 6 months

  2. Creatinine is concordant with venous blood sample

    Results match standard venous results for Creatinine and is within range: 52.2 - 119.3 micromoles/L.

    Time frame: 6 months

07

Study locations

1 site
  • Lancashire Teaching Hospitals NHS Foundation Trust
    Preston, Lancashire PR2 9HT, United Kingdom
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Feb 2024 (actual). Primary completion is estimated for Aug 2026, 30 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
May 31, 2024
First posted
Jun 6, 2024
StartActual
Feb 13, 2024
Primary completionEst.
Aug 31, 2026
CompletionEst.
Nov 30, 2026
Last update
Apr 8, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 8, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06445205
Lead sponsor
Lancashire Teaching Hospitals NHS Foundation Trust
Responsible party
Sponsor
First posted
Jun 6, 2024
Start date
Feb 13, 2024
Primary completion
Aug 31, 2026 (estimated)
Completion
Nov 30, 2026 (estimated)
Last update
Apr 8, 2025

Study contacts

Kina Bennett, PhD
study chair · Lancashire Teaching Hospitals NHS Foundation Trust

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is suspended, as verified in May 2024. You cannot join it, but the record below documents what was studied.

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