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Interaction between inulin supplementation and cyclophosphamide therapy in patients with breast cancer

Phase 2
Completed
Conditions
Breast cancer
Cachexy
Chemotherapy toxicity
Cancer - 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
NameTimeMethod
<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
NameTimeMethod
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