Tumour heterogeneity studies based on dedicated breast PET using proliferation radiotracers: early detection of the treatment response.
- Conditions
- Breast cancer
Recruitment & Eligibility
- Status
- Authorised, recruitment pending
- Sex
- Female
- Target Recruitment
- 100
-Adult women with breast cancer whose therapeutic plan is neoadjuvant chemotherapy
-Negative pregnancy test
-Information Sheet and Informed Consent Form signed by the patient
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 175
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
-Healthy women
-Women with breast cancer under 18
-Diabetic women with breast cancer
-Pregnant women with breast cancer
-Breast feeding women with breast cancer
-Women with breast cancer who have undergone a surgical procedure
-Women with breast cancer who have received chemotherapy or radiotherapy before the beginning of the study
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Complexo Hospitalario Universitario De Santiago
🇪🇸Santiago De Compostela, Spain
Complexo Hospitalario Universitario De Santiago🇪🇸Santiago De Compostela, SpainVirginia Pubul NúñezSite contact+34981951430virginia.pubul.nunez@sergas.es
