ClinicalTrials.gov record
Terminated Phase 4 Interventional Results available

L-Carnitine L-Tartrate in Preventing Peripheral Neuropathy Caused By Chemotherapy in Women With Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT00754767

Public ClinicalTrials.gov record NCT00754767. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 17, 2026, 4:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Pilot Study of L-Carnitine Supplementation in the Prevention of Chemotherapy-induced Peripheral Neuropathy in Women With Metastatic Breast Cancer

Study identification

NCT ID
NCT00754767
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
HealthPartners Institute
Other
Enrollment
2 participants

Conditions and interventions

Interventions

  • L-carnitine L-tartrate Drug
  • placebo Other

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 120 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 1, 2007
Primary completion
Apr 1, 2008
Completion
May 1, 2008
Last update posted
Sep 10, 2017

2007 – 2008

United States locations

U.S. sites
2
U.S. states
1
U.S. cities
2
Facility City State ZIP Site status
Masonic Cancer Center at University of Minnesota Minneapolis Minnesota 55455
Park Nicollet Cancer Center Saint Louis Park Minnesota 55426

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00754767, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 10, 2017 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00754767 live on ClinicalTrials.gov.

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