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Prevention of Paclitaxel-induced Peripheral Neuropathy in Breast Cancer Patients

Phase 2
Recruiting
Conditions
Peripheral Neuropathy Due to Chemotherapy
Registration Number
NCT06135493
Lead Sponsor
Future University in Egypt
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

Inclusion Criteria:<br><br> - Females older than 18 years diagnosed with biopsy-confirmed breast cancer (Early<br> breast cancer eligible for adjuvant or neoadjuvant) who are scheduled to receive<br> paclitaxel 80 mg/m2.<br><br>Exclusion Criteria:<br><br> - Known hypersensitivity to Losartan.<br><br> - Not Known Hypertensive patients<br><br> - Not Known Diabetic patients<br><br> - Treatment with Losartan/ARBs/ACE-I prior to the study.<br><br> - Previous neuropathy<br><br> - Renal impairment (Serum creatinine > 2 mg/dl)<br><br> - Significant liver disease: liver enzymes 2 folds the upper normal limit<br><br> - Metastatic breast cancer<br><br> - Pregnancy or lactation<br><br> - Taking other medication for neuropathic pain<br><br> - Significant Hypotension

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Development of paclitaxel-induced peripheral neuropathy;Grade of neuropathy
Secondary Outcome Measures
NameTimeMethod
Functional Assessment of Cancer Therapy/Gynecologic Oncology Group - Neurotoxicity (FACT/GOG-NTX);Biomarker
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