Last updated: January 22, 2024
Sponsor: Ain Shams University
Overall Status: Completed
Phase
2/3
Condition
Peripheral Neuropathy
Neurologic Disorders
Treatment
Placebo
Pentoxifylline
Paclitaxel
Clinical Study ID
NCT05189535
s2192648
Ages 18-80 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Adult patients (18-80 years old).
- Female patients.
- Pathologically proved breast cancer.
- Breast cancer patients who will receive adjuvant and neoadjuvant weekly paclitaxel for 12 weeks.
- Eastern Cooperative Oncology Group (ECOG) performance ≤ 2
- Adequate bone marrow function.
- Adequate liver and kidney function.
Exclusion
Exclusion Criteria:
- Patients with preexisting clinical neuropathy.
- Patients with diabetes mellitus.
- Metastatic breast cancer.
- Patients receiving medications that ameliorate neuropathy like; antidepressants,anticonvulsants, opioids, adjuvant or topical analgesics.
- Patients treated with medications that increase the risk of neuropathy.
- Hypersensitivity to pentoxifylline or xanthine derivatives.
- Patients with recent (within 1 month) surgery, myocardial infarction (MI),intracranial or retinal bleeding or active peptic ulcer.
- Patients at high risk for bleeding or taking medications that increase risk ofbleeding.
Study Design
Total Participants: 66
Treatment Group(s): 3
Primary Treatment: Placebo
Phase: 2/3
Study Start date:
October 03, 2021
Estimated Completion Date:
September 28, 2023
Study Description
Connect with a study center
Ain Shams University hospitals
Cairo, Abbasia 11566
EgyptSite Not Available

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