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Study of Hypoxia Measured in F-Miso PET/Scan and MRI in Patients With Squamous Cells Carcinoma (HYPONECK)

C

Centre Henri Becquerel

Status and phase

Unknown
Phase 2

Conditions

Squamous Cell Carcinoma of the Oropharynx

Treatments

Drug: F-Miso PET scan coupled with MRI

Study type

Interventional

Funder types

Other

Identifiers

NCT04031534
CHB16.03

Details and patient eligibility

About

Hypoxia imaging has not been studied extensively by combining PET and MRI data. Few studies performed the double imaging and none associated anatomopathology with it . This study will use a rigorous methodology through the production of PET/MRI images at the same time by transferring the patient directly from PET to MRI. In addition, the population, unlike other studies, will include preoperative patients with 24-hour surgery for hypoxia imaging by obtaining additional data through specific immunohistochemical analysis of hypoxia.

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient with squamous cells carcinoma of oropharynx
  • Age Superior to 10 years old
  • Male or Female
  • measurable target according RECIST criteria

Exclusion criteria

  • -Other histologic cancer than squamous cells carcinoma of oropharynx
  • No measurable target
  • Presence of metastasis

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Measure of hypoxia by F-Miso PET scan and RMI
Experimental group
Description:
Patient will undergo F-Miso PET scan and MRI to detect hypoxia. Imaging will be correlated with immunohistochemistry on tumour biopsy
Treatment:
Drug: F-Miso PET scan coupled with MRI

Trial contacts and locations

1

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Central trial contact

Sebastien Thureau, MD, PhD; Doriane Richard, PhD

Data sourced from clinicaltrials.gov

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