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Trials / Not Yet Recruiting

Not Yet RecruitingNCT07287592

Glutamine for the Prophylaxis of Vincristine-induced Neuropathy in Children and Adolescents With Cancer.

Glutamine for the Prophylaxis of Vincristine-induced Neuropathy in Children and Adolescents With Cancer. A Single Center Study

Status
Not Yet Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
Ain Shams University · Academic / Other
Sex
All
Age
6 Years – 18 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to assess the efficacy of glutamine in preventing the occurrence of vincristine induced neuropathy and to compare the reduction in rate of any dose reductions and premature chemotherapy discontinuation rates due to peripheral neuropathy between those who treated with glutamine and those who did not. Participants will: receive glutamine in a dose of 6 g /m2 twice daily (up to a maximum of 10 g/dose) for 14 consecutive days from d 1 of induction and 14 days from d1 of continuation . • Subjects will be asked to return for a complete study assessments visit every 14-days during supplementation period for a total of 4 visits Keep a diary of their symptoms of neuropathy and compliance to treatment and any adverse event

Conditions

Interventions

TypeNameDescription
DRUGGlutamine (Pharmacological doses)glutamine is an essential amino acid. It will be provided in a powder form. It will be dissolved in at least 8 ounces of hot or cold liquid. It can also be mixed with a soft food such as pudding

Timeline

Start date
2025-12-30
Primary completion
2026-12-30
Completion
2027-04-30
First posted
2025-12-17
Last updated
2025-12-17

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07287592. Inclusion in this directory is not an endorsement.