Clinical Trials Directory

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UnknownNCT04656782

EORTC-endorsed, Prospective European Multicenter Imaging Survey and Protocol

Towards Standardization of mCRC Imaging - an EORTC-endorsed, Prospective European Multicenter Imaging Survey and Imaging Protocol

Status
Unknown
Phase
Study type
Observational
Enrollment
40 (estimated)
Sponsor
Ludwig-Maximilians - University of Munich · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

A prospective, multicenter imaging Delphi survey among European radiological societies for mCRC imaging standardization.

Detailed description

BACKGROUND: Computed Tomography (CT) is the imaging reference standard for initial staging and response assessment in randomized, controlled clinical trials (RCT) dealing with metastatic colorectal cancer (mCRC). However, comparability of imaging data among recruiting centers in RCTs is highly hampered by diverging imaging protocols and different technical specifications. Over the last years, analysis of radiomic features in mCRC patients has gained increasing interest for image evaluation beyond the mere assessment of extent. Also, these radiomic features are highly susceptible to technical parameters such as slice thickness. Hence, comparability of radiomic features among recruiting centers are also highly limited due to diverging imaging protocols. AIMS: This prospective, multicenter imaging survey aims at assessing current differences regarding mCRC CT imaging protocols and technical specifications among large academic sites in Europe and at drafting a consensus imaging protocol endorsed by the European Organisation for Research and Treatment of Cancer (EORTC). METHODS: This survey will be in close cooperation of the EORTC Imaging Group, EORTC Gastro-intestinal Tract Group, European Society of Oncologic Imaging (ESOI) and European Society of Gastrointestinal and Abdominal Radiology (ESGAR). Among the EORTC Imaging Group, EORTC Gastro-intestinal Tract Group, ESOI and ESGAR, imaging experts will be prospectively recruited and will serve as expert panelists in this prospective survey. Following the Delphi approach for survey conduction, several survey rounds will be performed. The answers of each survey round will be analyzed by the survey facilitators, blinded results will then be forwarded to the expert panelists prior to every following survey round. Statements / answers can then be modified by the expert panelists in the following survey round.

Conditions

Interventions

TypeNameDescription
OTHERImaging surveyParticipation as expert panelist in the imaging survey.
OTHERFacilitationModeration and evaluation of the expert panel's answers. Adoption and moderation of further survey rounds.

Timeline

Start date
2021-01-26
Primary completion
2021-06-30
Completion
2021-12-31
First posted
2020-12-07
Last updated
2021-01-26

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT04656782. Inclusion in this directory is not an endorsement.