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Hormone Estradiol Replacement Therapy Additional Herbals
NCT02618148 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to determine whether Hormone Replacement Therapy (HRT), safety studies are combined with herbal (garlic oil, rutin, and nattokinase) to reduce estrogen side effects. Making it safer when an endocrine supplement is needed for estrogen deficiency symptoms in menopausal and postmenopausal women.
Conditions Studied
Interventions
- DRUG ESTROGEN HERBALS 21
- DRUG ESTROGEN HERBALS 28
Study Locations (2)
Delaware
- Saigon Biopharma LLC — Wilmington
Other
- Saigon Biopharma Company Limited — Ho Chi Minh City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2009-01 |
| Est. Completion | 2015-06 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02618148
The ClinicalTrials.gov registry entry for NCT02618148 describes a study currently listed as completed. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Trieu, Nguyen Thi, M.D., which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Menopause appearing as the primary indexed condition, and to 2 interventions — of which ESTROGEN HERBALS 21 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02618148 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Delaware, Other. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT02618148 about?
NCT02618148 is a clinical study titled "Hormone Estradiol Replacement Therapy Additional Herbals". The purpose of this study is to determine whether Hormone Replacement Therapy (HRT), safety studies are combined with herbal (garlic oil, rutin, and nattokinase) to reduce estrogen side effects. Making it safer when an endocrine supplement is needed for estrogen deficiency symptoms in menopausal and...
What is the current status of trial NCT02618148?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 60 participants. The study started on 2009-01. Estimated completion is 2015-06.
What conditions does trial NCT02618148 study?
This clinical trial studies the following conditions: Menopause. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02618148?
The interventions under investigation include: ESTROGEN HERBALS 21 (DRUG), ESTROGEN HERBALS 28 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02618148?
This trial is sponsored by Trieu, Nguyen Thi, M.D., which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02618148 being conducted?
This trial has 2 study locations across Delaware. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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