Clinical trial

Efficacy of Losartan in the Prevention of Paclitaxel-induced Peripheral Neuropathy in Breast Cancer Patients.

Name
REC-FPFUE-30/2023
Description
Paclitaxel-induced peripheral neuropathy (PIPN) is one of the most dose-limiting side effects; it causes patients discomfort and pain and sometimes causes the termination of the chemotherapy cycles, leading to treatment failure. A lot of interventions have been tried to prevent PIPN, ensure complete administration of the chemotherapy cycles, and increase the survival rate. One of the promising interventions in the prevention of PIPN is Losartan. Losartan is an angiotensin receptor blocker (ARBs) and is used to treat hypertensive patients. There is strong evidence from different preclinical studies and retrospective cohort studies that Losartan has a neuroprotective effect. The purpose of our study is to investigate the efficacy of Losartan in the prevention of peripheral neuropathy associated with Paclitaxel treatment in Breast Cancer patients.
Trial arms
Trial start
2023-12-12
Estimated PCD
2024-06-30
Trial end
2024-06-30
Status
Recruiting
Phase
Early phase I
Treatment
Losartan
Using losartan to prevent paclitaxel-induced peripheral neuropathy
Arms:
Intervention arm
Size
84
Primary endpoint
Development of paclitaxel-induced peripheral neuropathy
12 weeks
Grade of neuropathy
12 weeks
Eligibility criteria
Inclusion Criteria: * Females older than 18 years diagnosed with biopsy-confirmed breast cancer (Early breast cancer eligible for adjuvant or neoadjuvant) who are scheduled to receive paclitaxel 80 mg/m2. Exclusion Criteria: * Known hypersensitivity to Losartan. * Not Known Hypertensive patients * Not Known Diabetic patients * Treatment with Losartan/ARBs/ACE-I prior to the study. * Previous neuropathy * Renal impairment (Serum creatinine \> 2 mg/dl) * Significant liver disease: liver enzymes 2 folds the upper normal limit * Metastatic breast cancer * Pregnancy or lactation * Taking other medication for neuropathic pain * Significant Hypotension
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'PREVENTION', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 84, 'type': 'ESTIMATED'}}
Updated at
2024-03-20

1 organization

1 drug

1 indication