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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03004755
Other study ID # UCL/13/0165
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 2014
Est. completion date November 2023

Study information

Verified date February 2022
Source University College, London
Contact Abby Sharp
Phone 02076799688
Email ctc.peace@ucl.ac.uk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Historically, cancer research has been limited by sample acquisition in late stage disease, often restricted to single sites of disease with limited parallel clinical data collection in terms of prior therapy exposure. The PEACE study is intended to facilitate tissue donation from multiple tumour sites in the post-mortem setting and enable future research using samples collected at post-mortem within different disciplines related to cancer research.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date November 2023
Est. primary completion date November 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age 18 years or older - Confirmed diagnosis of any form of solid malignancy with metastatic disease (where the site of origin is known or unknown), with the exception of primary brain tumour in which there may not be evidence of metastatic disease - Oral and written informed consent from patient to enter the study and to undergo tumour harvesting after death or informed consent from a person in a qualifying relationship after the patient has died. Exclusion Criteria: - Medical or psychiatric condition that would preclude informed consent - History of intravenous drug abuse within the last 5 years - History of known high-risk infections (e.g. HIV/AIDS-positive, hepatitis B/C, tuberculosis and Creutzfeldt-Jacob disease).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Tissue Harvest


Locations

Country Name City State
United Kingdom Heart of England NHS Foundation Trust Birmingham
United Kingdom Cambridge University NHS Trust Cambridge
United Kingdom Greater Glasgow Health Board Glasgow
United Kingdom University Hospitals of Leicester NHS Trust Leicester
United Kingdom Guy's and St Thomas NHS Foundation Trust London
United Kingdom The Royal Marsden NHS Foundation Trust London
United Kingdom University College London Hospitals NHS Foundation Trust London
United Kingdom The Christie NHS Foundation Trust Manchester
United Kingdom Oxford University Hospitals NHS Trust Oxford

Sponsors (2)

Lead Sponsor Collaborator
University College, London Cancer Research UK

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perform 500 post mortems 5 years
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