A Phase I/II Imaging Study of 1-a-D-(5-deoxy-5-[18]F-fluoroarabinofuranosyl)-2-nitroimidazole ([18]F-FAZA) in Patients With Known Squamous Cell Carcinoma of the Head & Neck, Small Cell and Non-Small Cell Carcinoma of the Lung, Lymphoma, Glioblastoma Multiforme, Neuroendocrine Tumours or Renal Cell Carcinoma
18F-FAZA PET Imaging
Urogenital Diseases+17
+ Adenocarcinoma
+ Carcinoma
Diagnostic Study
Summary
Study start date: September 12, 2006
Actual date on which the first participant was enrolled.This is a diagnostic study that focuses on a specific type of imaging called 18F-FAZA PET scan. The study involves patients who have been diagnosed with certain types of cancer, including squamous cell carcinoma of the Head & Neck, small cell and non-small cell carcinoma of the lung, lymphoma, glioblastoma multiforme, neuroendocrine tumors, or renal cell carcinoma. The main goal of this study is to ensure the safety of 18F-FAZA, a substance used in the imaging process, and to understand how it spreads within the body. This research is important as it could potentially improve the way these cancers are diagnosed and treated. The study consists of two phases. In the first phase, patients will undergo a single 18F-FAZA PET scan. Their vital signs, blood test results, and any adverse events will be carefully monitored before the injection and after the imaging. In the second phase, patients will receive three 18F-FAZA PET scans: one before treatment, one during the middle of the treatment, and one after the treatment. The study will examine where the 18F-FAZA goes in the body and how much is taken up by normal and abnormal tissues.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.92 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Diagnostic Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 16 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location