Clinical TrialID 1240

Safety Study of Black Cohosh Use by Postmenopausal Women on the Liver

NCT00794690

Menopause

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
1240
Evidence Id
1240
Core Evidence Id
1240
Source Clinical Trial Id
1223
Herb2 Clinical Trial Id
HBCT001223
Nct Id
NCT00794690
Title
Safety Study of Black Cohosh Use by Postmenopausal Women on the Liver
Status
Completed
Phase
Study Result
No
Study Condition
Menopause
Study Type
Interventional
Study Design
Allocation: NON_RANDOMIZED|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Intervention
DRUG: Cimicifuga racemosa extract for the group
Intervention Allocation
Non_Randomized
Intervention Model
Single_Group
Intervention Mask
Intervention Purpose
Treatment
Gender
Female
Age
Adult, Older_Adult
Enrollment
100
Outcome Measure
Effect on hepatic perfusion and liver functions, 12 months
Sponsor Collaborator
Assiut University
Funded By
OTHER
Location
Dept. Obstetrics and Gynecology, Assiut University, Assiut, 71516, Egypt
Other Id
CR and the liver
Start Date
2008-01
Primary Completion Date
2008-12
Completion Date
2009-01
First Posted
2008-11-20
Results First Posted
Last Update Posted
2009-08-03
Study Document
Study Url
https://clinicaltrials.gov/study/NCT00794690
Title Cn
Title En
Safety Study of Black Cohosh Use by Postmenopausal Women on the Liver
Bilingual Status
semi_complete