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Investigating the effect of Curcumin on vincristine-induced neuropathy

Investigating the effect of oral Curcumin on vincristine-induced neuropathy in children with Acute lymphoblastic leukemia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201107049296N3
Enrollment
140
Registered
2023-10-16
Start date
2022-09-11
Completion date
Unknown
Last updated
2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neuropathy. Drug-induced polyneuropathy

Interventions

Intervention 1: Intervention group: Patients received one oral capsule of Curcumin (manufactured by Dineh Company, Iran) every 12 hours (with a dose of 3 mg/kg) for 3 months. Intervention 2: Placebo g

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 18 Years

Inclusion criteria

Inclusion criteria: Consent of parents or children older than 13 years to participate in the study Age range from 5 to 18 years Children who have recently been diagnosed with ALL and have not yet started treatment with vincristine

Exclusion criteria

Exclusion criteria: Congenital malformations and developmental disoreders Primary central nervous system involvement History of taking anti-inflammatory and antioxidant drugs Under treatment with other drugs leading to nephropathy Presence of neuropathy before treatment with vincristine

Design outcomes

Primary

MeasureTime frame
Presence or absence of neuropathy. Timepoint: Before intervention and 3 months after the intervention. Method of measurement: EMG, NCV and the 12 canial nerve examinations.

Secondary

MeasureTime frame
Severity of neuropathy. Timepoint: Before intervention and 3 months after the intervention. Method of measurement: EMG, NCV and clinical examinations of 12 nerves.

Countries

Iran (Islamic Republic of)

Contacts

Public Contact?Aziz Eghbali

Iran University of Medical Sciences

eghbali.a@iums.ac.ir+98 21 2222 2041

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 5, 2026