neuropathy.
Conditions
Interventions
Intervention 1: Intervention group: Patients treated with bortezomibe with a dose of 1.3 mg per m2 and vitamin B1 simultaneously. (Vitamin B1 at a dose of 300 mg per day orally). Intervention 2: Contr
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: who were suspected to receive Bortezomib based chemotherapy regimen
Exclusion criteria
Exclusion criteria: do not have interfering factors such as: Previous history of symptomatic peripheral neuropathy, Diabetes mellitus, End stage renal disease, history of alcohol abuse, and any other neuromuscular disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Neuropathy. Timepoint: 4month. Method of measurement: experimental symptom-based questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactGhazal Rafiaei
Esfahan University of Medical Sciences
Outcome results
None listed