Clinical TrialID 1164

Clinical Trial of Trametes Versicolor in Women With Breast Cancer

NCT00680667

Breast Cancer

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
1164
Evidence Id
1164
Core Evidence Id
1164
Source Clinical Trial Id
1146
Herb2 Clinical Trial Id
HBCT001146
Nct Id
NCT00680667
Title
Clinical Trial of Trametes Versicolor in Women With Breast Cancer
Status
Completed
Phase
Phase 1
Study Result
No
Study Condition
Breast Cancer
Study Type
Interventional
Study Design
Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Intervention
BIOLOGICAL: Coriolus versicolor extract
Intervention Allocation
Intervention Model
Single_Group
Intervention Mask
Intervention Purpose
Treatment
Gender
Female
Age
Adult, Older_Adult
Enrollment
11
Outcome Measure
Maximum tolerated dose, Up to 6 Weeks After Treatment
Sponsor Collaborator
Masonic Cancer Center, University of Minnesota|National Center for Complementary and Integrative Health (NCCIH)
Funded By
OTHER
Location
Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota, 55455, United States|Bastyr University, Kenmore, Washington, United States
Other Id
2007LS019|U19AT001998|UMN-0611M96168
Start Date
2007-04
Primary Completion Date
2011-04
Completion Date
2011-04
First Posted
2008-05-20
Results First Posted
Last Update Posted
2017-11-29
Study Document
Study Url
https://clinicaltrials.gov/study/NCT00680667
Title Cn
Title En
Clinical Trial of Trametes Versicolor in Women With Breast Cancer
Bilingual Status
semi_complete