MedPath

Tumour heterogeneity studies based on dedicated breast PET using proliferation radiotracers: early detection of the treatment response.

Phase 1/2
Not yet recruiting
Conditions
Breast cancer
Registration Number
2024-512152-38-00
Lead Sponsor
Fundacion Instituto De Investigacion Sanitaria De Santiago De Compostela
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised, recruitment pending
Sex
Female
Target Recruitment
100
Inclusion Criteria

-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

Exclusion Criteria

-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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Complexo Hospitalario Universitario De Santiago

🇪🇸

Santiago De Compostela, Spain

Complexo Hospitalario Universitario De Santiago
🇪🇸Santiago De Compostela, Spain
Virginia Pubul Núñez
Site contact
+34981951430
virginia.pubul.nunez@sergas.es

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.