Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02215083

L-glutamine Supplementation to Alleviate Symptoms of Taxane-Induced Neuropathy in Patients With Breast Cancer

Status
Withdrawn
Phase
Phase 1
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Eastern Regional Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to determine whether daily, high-dose administration of l-glutamine can reduce numbness and tingling caused by a taxane chemotherapy in patients with breast cancer.

Detailed description

L-glutamine has previously been shown to help reduce the incidence of numbness and tingling in patients with breast cancer who are receiving taxane chemotherapies. However, no study to date looks at the effect of l-glutamine given after this numbness and tingling (called 'perihperhal neuropathy') has already occurred. We hypothesize that administration of this amino acid in l-glutamine naïve patients will result in a measureable reduction of their taxane-induced neuropathy.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTL-glutamine10,000mg by mouth, twice daily for nine weeks (± 7 days) with one permitted dose escalation to a maximum of 10,000mg by mouth three times daily.

Timeline

Start date
2014-08-01
Primary completion
2015-04-01
Completion
2015-04-01
First posted
2014-08-13
Last updated
2017-07-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02215083. Inclusion in this directory is not an endorsement.