CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 226 enrolled
Drug / intervention
Ginkgo Biloba +1 moredrug
Likely dose
Ginkgo Biloba 120 mg per day (60 mg twice daily)AI-extracted
Key inclusion· 7
  • Newly diagnosed breast cancer
  • Planned to receive standard adjuvant chemotherapy with or without a taxane
  • Age 18 or older
  • Female
Key exclusion· 13
  • Diabetes
  • Dementia
  • Psychiatric disorder diagnosed within the past 5 years that would preclude study compliance
  • Significant comorbidity

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00046891
NCT00046891Phase 3Completed

The Use of Ginkgo Biloba For The Prevention Of Chemotherapy-Related Cognitive Dysfunction

Alliance for Clinical Trials in Oncology·interventional·Posted Jan 27, 2003·Updated Jul 6, 2016

In Brief

A Phase 3 clinical trial evaluating Ginkgo Biloba and Placebo for Breast Cancer and Neurotoxicity. Completed, enrolled 226 participants across 175 sites.

Detailed Summary

RATIONALE: Chemotherapy may cause memory loss, attention loss, and other problems that make it difficult for patients to think clearly. EGb761 may help maintain mental clarity in patients undergoing chemotherapy. PURPOSE: Randomized clinical trial to study the effectiveness of EGb761 in preventing loss of mental clarity in women who are receiving chemotherapy for newly diagnosed breast cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 3CompletedFinished
2003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJan 27, 2003
Enrollment StartDec 1, 2002
Primary CompletionOct 1, 2006
Study CompletionApr 1, 2015
TodayJul 2, 2026
Enrollment to primary: 3.8 yearsPosted 23.4 years ago

Interventions

Ginkgo Bilobadrug

Patients will take 120 mg per day (60 mg BID)

Placeboother

Patients will take 1 tablet BID