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NCT00066144 · ClinicalTrials.gov registry record · Phase 2
Use of Black Cohosh and Red Clover for the Relief of Menopausal Symptoms
A Phase 2 study of Menopause and Hot Flashes, sponsored by National Center for Complementary and Integrative Health (NCCIH).
- Completed
- Registry status
- Phase 2
- Development phase
- 112
- Enrollment target
- 1
- Study location
NCT00066144 is a Phase 2 study of Menopause and Hot Flashes that has completed, run by National Center for Complementary and Integrative Health (NCCIH). The registered enrollment target is 112 participants, below the 9,392-participant average among 54 other Menopause trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00066144, a Phase 2 study of Menopause and Hot Flashes, has completed, sponsored by National Center for Complementary and Integrative Health (NCCIH).
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 112 participants
- Enrollment target
- 1
- Study location
Study Summary
This Phase II study, a follow-up to a Phase I trial in normal volunteers, will determine the efficacy of black cohosh and red clover for the relief of menopausal symptoms. It will also assess the safety of chronic dosing (1 year) by evaluating uterine (endometrial biopsies), breast (mammography), and hematology parameters (CBC and chemistry lab values) at baseline and 1 year.
Conditions Studied
Interventions
- DRUG Cimicifuga racemosa
- DRUG Trifolium pratense
- DRUG Black cohosh
- DRUG Red clover
Study Locations (1)
Illinois
- University of Illinois at Chicago - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 112 participants |
| Start Date | 2003-04 |
| Est. Completion | 2006-04 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00066144
The ClinicalTrials.gov registry entry for NCT00066144 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 112 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 9,392-participant average among 54 other Menopause trials with a reported enrollment target (99% lower). The listed sponsor is National Center for Complementary and Integrative Health (NCCIH), which has 203 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Menopause appearing as the primary indexed condition, and to 4 interventions - of which Cimicifuga racemosa is the first listed.
NCT00066144 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.
Frequently Asked Questions
What is clinical trial NCT00066144 about?
NCT00066144 is a clinical study titled "Use of Black Cohosh and Red Clover for the Relief of Menopausal Symptoms". This Phase II study, a follow-up to a Phase I trial in normal volunteers, will determine the efficacy of black cohosh and red clover for the relief of menopausal symptoms. It will also assess the safety of chronic dosing (1 year) by evaluating uterine (endometrial biopsies), breast (mammography), an...
What is the current status of trial NCT00066144?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 112 participants. The study started on 2003-04. Estimated completion is 2006-04.
What conditions does trial NCT00066144 study?
This clinical trial studies the following conditions: Menopause, Hot Flashes.
What interventions are being tested in trial NCT00066144?
The interventions under investigation include: Cimicifuga racemosa (DRUG), Trifolium pratense (DRUG), Black cohosh (DRUG), Red clover (DRUG).
Who is sponsoring clinical trial NCT00066144?
This trial is sponsored by National Center for Complementary and Integrative Health (NCCIH), which has 203 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00066144 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.