Verified by Rambam Health Care Campus October 2005
|
Purpose
|
Condition | Intervention | Phase |
---|---|---|
Breast Cancer | Behavior: Lifemel honey intake every day | Phase II |
MedlinePlus related topics: Breast Cancer
Genetics Home Reference related topics: breast cancer
Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Lifemel Honey During Adjuvant Chemotherapy for Breast Cancer Patients to Prevent Leucopenia
Further study details as provided by Rambam Health Care Campus: Primary Outcomes: Prevention of myelotoxicity-every week during chemotherapy.
Expected Total Enrollment: 60
Study start: November 2005
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Female Criteria
Inclusion Criteria:
- breast cancer patient treated with adjuvant chemotherapy
- PS = 2 or less
Exclusion Criteria:
- none
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00243165
Georgeta Fried, MD 972-4-8543018 [email protected]
Study chairs or principal investigators
Georgeta Fried, MD, Principal Investigator, Rambam Health Care Campus
More Information
Study ID Numbers: LifemelCTIL
Last Updated: December 8, 2005
Record first received: October 20, 2005
ClinicalTrials.gov Identifier: NCT00243165
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration
ClinicalTrials.gov processed this record on 2006-01-10
Source: ClinicalTrials.gov