Ireland
--:--IST
Latest
Clinical Trials in Canada / NCT03176836
Enrolling by invitation Not applicable

Li-Fraumeni Syndrome Imaging Study

NCT03176836 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2016-06-20
Last updated
2026-04-29

Condition(s) studied

Li-Fraumeni Syndrome

Investigational drug(s) / intervention(s)

Whole body STIR MRIDW-MRIPET-MRI

Whole body STIR MRI: Standard technique that detects abnormalities related to excess of water in tissues (edema).

DW-MRI: MRI technique that analyzes areas of dead cells within tissues, present in some types of tumor.

PET-MRI: MRI technique that detect's the cells' use of glucose, more intensely in harmful cells.

Study summary

Li-Fraumeni Syndrome (LFS) is a cancer predisposition disorder in which most affected individuals develop cancer during their lifetime. The majority of LFS patients carry a mutation in a gene called TP53, whose normal function is to control cell growth and prevent cells with damaged DNA from becoming cancerous. There is currently no way to determine when, where or what type of tumour will develop. This project will use novel techniques utilizing magnetic resonance imaging (MRI) to determine how sensitive they are at detecting very small tumors and how specific they are in terms of distinguishing malignant tumors from benign tumors.

Eligibility

Sex
ALL
Min age
—
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: * LFS kindreds who either carry a known TP53 mutation or are obligate mutation carriers Exclusion Criteria: * General contraindications for an MRI scan (ferromagnetic prostheses, pacemaker, or other implants incompatible with the magnetic field of the MR scanner), claustrophobia.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The Hospital for Sick Children Toronto Ontario

More The Hospital for Sick Children trials in Canada

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03176836 on ClinicalTrials.gov ↗ ← All trials in Canada