Actively Recruiting

Phase Not Applicable
Age: 16Years +
All Genders
NCT02246634

Screening for Synchronous Metastases in Colorectal Cancer With DW-MRI (SERENADE)

Led by Imperial College London · Updated on 2024-10-17

282

Participants Needed

13

Research Sites

904 weeks

Total Duration

On this page

Sponsors

I

Imperial College London

Lead Sponsor

P

Pelican Cancer Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

Eligible patients with high risk colorectal malignancy (T3/4, spread greater than 5mm, EMVI positive) will have additional surveillance of breath hold T1, T2 and DW-MRIs (no IV contrast) post surgery six monthly for three years. Findings of liver MRIs as reported by radiology PI will be shared with their local MDT who make decisions as appropriate, including the management of any identified liver metastases, according to local protocol.

CONDITIONS

Official Title

Screening for Synchronous Metastases in Colorectal Cancer With DW-MRI (SERENADE)

Who Can Participate

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have a high risk primary colorectal malignancy
  • Have a negative CT or no confirmatory evidence of liver metastases
  • Are able to undergo treatment if liver metastasis is found
  • Have provided written informed consent to participate in the study
  • Be aged 16 years or over
Not Eligible

You will not qualify if you...

  • Have had a previous colorectal malignancy
  • Have metastatic disease
  • Have a synchronous second malignancy
  • Are contraindicated for MRI
  • Have a T3b or below low rectal tumour without EMVI or N1c

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 13 locations

1

Macclesfield District General Hospital

Macclesfield, Cheshire, United Kingdom, SK10 3BL

Actively Recruiting

2

Queen's Hospital

Burton-on-Trent, Derbyshire, United Kingdom, DE13 0RB

Not Yet Recruiting

3

Broomfield Hospital

Chelmsford, Essex, United Kingdom, CM1 7ET

Actively Recruiting

4

Royal Bolton Hospital

Bolton, Greater Manchester, United Kingdom, BL4 0JR

Actively Recruiting

5

Medway Maritime Hospital

Gillingham, Kent, United Kingdom, ME7 5NY

Actively Recruiting

6

University Hospital of South Manchester & Manchester Royal Infirmary

Wythenshawe, Manchester, United Kingdom, M23 9LT

Actively Recruiting

7

Royal Liverpool Hospital

Liverpool, Merseyside, United Kingdom, L7 8XP

Actively Recruiting

8

Royal Stoke University Hospital

Stoke-on-Trent, Staffordshire, United Kingdom, ST4 6QG

Actively Recruiting

9

Royal Marsden Hospital

Sutton, Surrey, United Kingdom, SM2 5PT

Actively Recruiting

10

Royal Gwent Hospital

Newport, Wales, United Kingdom, NP20 2UB

Actively Recruiting

11

George Eliot Hospital

Nuneaton, Warwickshire, United Kingdom, CV10 7DJ

Actively Recruiting

12

Salisbury District Hospital

Salisbury, Wiltshire, United Kingdom, SP2 8BJ

Actively Recruiting

13

Queen Alexandra Hospital

Portsmouth, United Kingdom

Actively Recruiting

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Research Team

C

Caroline Martin

CONTACT

S

Syvella Ellis

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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