Interaction between inulin supplementation and cyclophosphamide therapy in patients with breast cancer
Phase 2
Completed
- Conditions
- Breast cancerCachexyChemotherapy toxicityCancer - Breast
- Registration Number
- ACTRN12616001532493
- Lead Sponsor
- niversidad Autonoma del Estado de Mexico- Facultad de Medicina
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Patients with clinical diagnosis of breast cancer, with score 0 according to the scale Eastern Cooperative Oncology Group (ECOG) .
Patients who agree to participate and provide the required information.
Patients with chemotherapy scheme with cyclophosphamide alone or in combination with methotrexate, 5-fluorouracil and doxorubicin.
Exclusion Criteria
Patients with an ECOG score greater than or equal to 1.
Patients who do not sign informed consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <br> The change in GSTP1 mRNA expression in lymphocytes will be analyzed by qPCR.[Measures will be perfomed previuosly (day 0) and after inulin supplementation (21 days).<br> ]<br> ;<br> The change in GSTM1 mRNA expression in lymphocytes will be analyzed by qPCR.[Measures will be perfomed previuosly (day 0) and after inulin supplementation (21 days).<br> ]<br> ;<br> The change in GSTT1 mRNA expression in lymphocytes will be analyzed by qPCR.[Measures will be perfomed previuosly (day 0) and after inulin supplementation (21 days).<br> ]<br>
- Secondary Outcome Measures
Name Time Method