METEL Study Which is to Collect Urine Samples From Patients to Analyse Their Chemistry to Assess How Close to Death the Patient is at Point of Sample When They Have a Solid Cancer Tumour Diagnosis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThe Clatterbridge Cancer Centre NHS Foundation Trust

About this trial

Use of samples from patients with solid cancer tumour diagnosis to assess chemistry

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Must have as solid cancer tumour diagnosis Must be over the age of 18 Must be able to understand and communicate in English Must be able to provide fully informed consent at the point of trial entry Must be able to urinate freely or be catheterised

Disqualifiers

Does not have a solid cancer tumour diagnosis Under the age of 18 Unable to communicate and understand English Unable to provide fully informed consent at the point of trial entry Is no cathetherised or able to urinate freely

Trial population

Patients with a solid tumour cancer diagnosis

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

1,327 Participants
are grouped into 1 trial group
Group A: Solid Tumour Cancer

Trial outcomes

Primary outcomes

1

Study Outcome

This work could identify mechanisms involved in the dying process and develop test predicting time until death. Understanding of the biology of dying will improve the recognition of people in the last days and weeks of life. This will; - - Improve the quality of a person's death by reducing uncertainty and facilitating preferred place of care. Reduce healthcare spending on futile diagnostic and therapeutic interventions. We will correct urine samples once per week from participants, to be able to analyse their metabolites for changes towards end of life.

Time frame
18 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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