The i4i PRODICT® Study: Evaluation of the i4i PRODICT® Test in Different Ethnic Groups (The i4i PRODICT® Study).
About this study
The i4i PRODICT® study has been developed to investigate the uptake and acceptability of the i4i PRODICT® test which combines both common and rare genetic changes (genetic variants) into one saliva-based DNA test to estimate a person's future risk of prostate cancer (PrCa) in people of varying ethnicities.
- Condition
- Prostate Cancer
- Tested
- The i4i PRODICT® test., Prostate cancer screening, MRI Scan, Prostate Biopsy
- Sponsor
- Institute of Cancer Research, United Kingdom
Who can join
- Age
- 40 to 55 years
- Sex
- Male only
- Healthy volunteers
- Accepted
Inclusion 8
- Minimum age: 40 years
- Maximum age: 55 years
- Eligible sex: Male
- Study condition: Prostate Cancer
- People with a prostate\* (PwP). \*People with a prostate is defined as people born male.
- Aged 40 to 55 years.
- People of either (i) Black African/Black African-Caribbean; (ii) White European; or (iii) South Asian or East Asian ancestry. These are defined as individuals with 4 grandparents of the same ancestry.
- Absence of any psychological, familial, sociological or geographical situation potentially hampering compliance with the study protocol and follow-up schedule.
Exclusion 5
- Previous diagnosis of prostate cancer.
- People of mixed ancestry
- Previous diagnosis of cancer with a life-expectancy of less than five years.
- Negative prostate biopsy within one year before recruitment.
- Any significant psychological conditions that may be worsened or exacerbated by participation in the study.
Where
3 sites, 3 recruiting
The Royal Marsden Hospital
London, United Kingdom
The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust
Sutton, Surrey, United Kingdom
The Royal Marsden Hospital
Sutton, United Kingdom
Contact
-
Eva McGrowder, PhD
+44 208 722 4483 Eva.McGrowder@icr.ac.uk
-
Elizabeth K Bancroft, PhD
+44 208 722 4483 elizabeth.bancroft@rmh.nhs.uk
Potential match only. Final eligibility is determined by the study team.