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Value of Analysing Under-utilised Leftover Tissue (VauLT)

Sponsor: Royal Marsden NHS Foundation Trust

NCT ID: NCT03832062

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Leftover surgical tissue homogenization (other)
How long the study runs
Study runs about 123 months (dates as stated)
About the drug or intervention
Leftover surgical tissue homogenization — other: Leftover surgical tissue homogenization
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
800
Started
2018-09-10
Last checked
2025-05

Plain English Summary

What is this study?

  • • Testing a new treatment for oncology
  • • Clinical study - 800 participants
  • • Intratumour heterogeneity is well recognized in multiple cancer types and ultimately leads to therapeutic resistance

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with oncology

Where?

  • • London - Royal Marsden Hospital NHS Foundation Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Intratumour heterogeneity is well recognized in multiple cancer types and ultimately leads to therapeutic resistance. It also limits the ability of small samples to represent the whole tumour, having implications for diagnosis, molecular analysis and understanding of the tumour immune microenvironment. By blending- 'homogenizing'- leftover tumour tissue in excess of that required for diagnosistic purposes, one may create a more representative sample for analysis.

More detail

In order to establish the feasibility of homogenization as a potential companion diagnostic tool, our study aims to 1) evaluate how many surgical cases have left over tissue amenable to homogenization and 2) pilot homogenization across multiple tumour types. The molecular profile of the homogenate will be compared to that obtained from the diagnostic specimen using next generation sequencing techniques.

Oncology

How this trial compares with your answers

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What we know so far

Condition· Matched your search
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Still need:

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Leftover formalin-fixed tissue (ie that would be otherwise discarded by histopathology) from cancer surgery.
  • ✓Tissues for Research consent has been provided.
  • ✓Patient age \>18yo.
  • ✓Minimum of 1 gram of residual tumour remaining in leftover surgical tissue
  • ✓Minimum of 1 gram of normal tissue present.

Who cannot take part

  • ✗Advanced Practitioner in histological dissection deems tumour sample to be inadequate.
  • ✗Leftover surgical tumour tissue greater than 20kg.
See the full criteria
Inclusion Criteria: 1. Leftover formalin-fixed tissue (ie that would be otherwise discarded by histopathology) from cancer surgery. 2. Tissues for Research consent has been provided. 3. Patient age \>18yo. 4. Minimum of 1 gram of residual tumour remaining in leftover surgical tissue 5. Minimum of 1 gram of normal tissue present. Exclusion Criteria: 1. Advanced Practitioner in histological dissection deems tumour sample to be inadequate. 2. Leftover surgical tumour tissue greater than 20kg.

Where Is This Study? (1 UK site)

Royal Marsden Hospital NHS Foundation Trust

London SW3 6JJ, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Serena Vanzan

Sponsor contact

CONTACT

020 3186 5161 vault@rmh.nhs.uk

Eleanor Carlyle

Sponsor contact

CONTACT

Renal&Melanoma.researchteam@rmh.nhs.uk
Data sourced from ClinicalTrials.gov · Last verified: 2025-05