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NCT02710214 · ClinicalTrials.gov registry record · Phase 2
A TSEC for Symptom Management in Menopausal Women With Multiple Sclerosis
A Phase 2 study of Multiple Sclerosis and Menopause, sponsored by University of California, San Francisco.
- Completed
- Registry status
- Phase 2
- Development phase
- 24
- Enrollment target
- 1
- Study location
NCT02710214 is a Phase 2 study of Multiple Sclerosis and Menopause that has completed, run by University of California, San Francisco. The registered enrollment target is 24 participants, below the 585-participant average among 315 other Multiple Sclerosis trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02710214, a Phase 2 study of Multiple Sclerosis and Menopause, has completed, sponsored by University of California, San Francisco.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 24 participants
- Enrollment target
- 1
- Study location
Study Summary
Duavee is a hormone receptor modulator that has been approved for the treatment of menopausal symptoms in menopausal women. The goal of this 8-week randomized, double blind, placebo controlled pilot study, is to determine whether this medication alleviates menopausal symptoms in women with MS. The investigators will secondarily determine whether addressing menopausal symptoms ameliorates MS symptoms and, on MRIs, is not triggering worsening inflammation.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Tissue Selective Estrogen Complex
Study Locations (1)
California
- University of California, San Francisco - San Francisco
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2016-02 |
| Est. Completion | 2019-04-24 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02710214
The ClinicalTrials.gov registry entry for NCT02710214 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 585-participant average among 315 other Multiple Sclerosis trials with a reported enrollment target (96% lower). The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Multiple Sclerosis appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT02710214 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT02710214 about?
NCT02710214 is a clinical study titled "A TSEC for Symptom Management in Menopausal Women With Multiple Sclerosis". Duavee is a hormone receptor modulator that has been approved for the treatment of menopausal symptoms in menopausal women. The goal of this 8-week randomized, double blind, placebo controlled pilot study, is to determine whether this medication alleviates menopausal symptoms in women with MS. The i...
What is the current status of trial NCT02710214?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 24 participants. The study started on 2016-02. Estimated completion is 2019-04-24.
What conditions does trial NCT02710214 study?
This clinical trial studies the following conditions: Multiple Sclerosis, Menopause.
What interventions are being tested in trial NCT02710214?
The interventions under investigation include: Placebo (DRUG), Tissue Selective Estrogen Complex (DRUG).
Who is sponsoring clinical trial NCT02710214?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02710214 being conducted?
This trial has 1 study location across California. 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
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