The PEACE (Posthumous Evaluation of Advanced Cancer Environment) Study (PEACE)
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT03004755 |
Recruitment Status :
Recruiting
First Posted : December 29, 2016
Last Update Posted : February 23, 2022
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Condition or disease | Intervention/treatment |
---|---|
Solid Tumor, Adult Cancer | Other: Tissue Harvest |
Study Type : | Observational |
Estimated Enrollment : | 500 participants |
Observational Model: | Cohort |
Time Perspective: | Prospective |
Official Title: | The PEACE (Posthumous Evaluation of Advanced Cancer Environment) Study |
Study Start Date : | March 2014 |
Estimated Primary Completion Date : | November 2023 |
Estimated Study Completion Date : | November 2023 |
- Perform 500 post mortems [ Time Frame: 5 years ]

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
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).

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03004755
Contact: Abby Sharp | 02076799688 | ctc.peace@ucl.ac.uk |
United Kingdom | |
Heart of England NHS Foundation Trust | Recruiting |
Birmingham, United Kingdom | |
Cambridge University NHS Trust | Recruiting |
Cambridge, United Kingdom | |
Greater Glasgow Health Board | Recruiting |
Glasgow, United Kingdom | |
University Hospitals of Leicester NHS Trust | Recruiting |
Leicester, United Kingdom | |
Guy's and St Thomas NHS Foundation Trust | Recruiting |
London, United Kingdom | |
The Royal Marsden NHS Foundation Trust | Recruiting |
London, United Kingdom | |
University College London Hospitals NHS Foundation Trust | Recruiting |
London, United Kingdom | |
The Christie NHS Foundation Trust | Recruiting |
Manchester, United Kingdom | |
Oxford University Hospitals NHS Trust | Not yet recruiting |
Oxford, United Kingdom |
Responsible Party: | University College, London |
ClinicalTrials.gov Identifier: | NCT03004755 |
Other Study ID Numbers: |
UCL/13/0165 |
First Posted: | December 29, 2016 Key Record Dates |
Last Update Posted: | February 23, 2022 |
Last Verified: | February 2022 |