Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Trial: 1Ingredient: 1Links: 1
Arranging relationship network...
Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 2428
- Evidence Id
- 2428
- Core Evidence Id
- 2428
- Source Clinical Trial Id
- 2405
- Herb2 Clinical Trial Id
- HBCT002405
- Nct Id
- NCT00908570
- Title
- Topical Estriol for Vaginal Health
- Status
- Completed
- Phase
- Phase 1
- Study Result
- No
- Study Condition
- Vaginal Health
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, CARE_PROVIDER)|Primary Purpose: PREVENTION
- Intervention
- DRUG: estriol|DRUG: Placebo
- Intervention Allocation
- Randomized
- Intervention Model
- Parallel
- Intervention Mask
- Double
- Intervention Purpose
- Prevention
- Gender
- Female
- Age
- Adult
- Enrollment
- 104
- Outcome Measure
- Change in thickness of the vaginal epithelium, Pre and post treatment luteal and follicular phases
- Sponsor Collaborator
- Gynuity Health Projects|University of Illinois at Chicago|University of California, Los Angeles|Tulane University School of Medicine|Magee-Women's Research Institute|Oregon Health and Science University
- Funded By
- OTHER
- Location
- Harbor-UCLA Medical Center, Los Angeles, California, 90502, United States|University of Illinois at Chicago, Chicago, Illinois, 60612, United States
- Other Id
- 5.1
- Start Date
- 2009-06
- Primary Completion Date
- 2011-03
- Completion Date
- 2011-03
- First Posted
- 2009-05-27
- Results First Posted
- Last Update Posted
- 2011-03-04
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT00908570
- Title Cn
- Title En
- Topical Estriol for Vaginal Health
- Bilingual Status
- semi_complete