Clinical Trials Directory

Trials / Completed

CompletedNCT00135161

Feasibility Study of Incorporating 18F-FDG-PET Imaging in Radiotherapy for Head and Neck Cancer

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
University Hospital, Ghent · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this trial is to study fluorodeoxyglucose-positron emission tomography (FDG-PET)-based dose escalation using intensity modulated radiation therapy (IMRT).

Detailed description

The dose escalation, based on the FDG-PET signal, is incorporated in the first ten fractions of the radiotherapeutic treatment. The total amount of fractions is 32, equal to a standard radiotherapeutic treatment for these types of cancers.

Conditions

Interventions

TypeNameDescription
PROCEDUREFDG-PET-based dose escalation using intensity modulated radiation therapy (IMRT).FDG-PET-based dose escalation using intensity modulated radiation therapy (IMRT).

Timeline

Start date
2003-09-01
Primary completion
2015-08-01
Completion
2015-08-01
First posted
2005-08-25
Last updated
2022-12-08

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT00135161. Inclusion in this directory is not an endorsement.

Feasibility Study of Incorporating 18F-FDG-PET Imaging in Radiotherapy for Head and Neck Cancer (NCT00135161) · Clinical Trials Directory