Page last updated: 2024-11-06

estriol and Demyelinating Diseases

estriol has been researched along with Demyelinating Diseases in 1 studies

hormonin: estrogen replacement; each tablet contains 600 ug micronized 17beta-estradiol, 270 ug estriol and 1.4 mg estrone
chlorapatite : A phosphate mineral with the formula Ca5(PO4)3Cl.

Demyelinating Diseases: Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system.

Research Excerpts

ExcerptRelevanceReference
"Estriol treatment prevented decreases in excitatory synaptic transmission and lessened the effect of EAE on PPF."1.38Estriol preserves synaptic transmission in the hippocampus during autoimmune demyelinating disease. ( Avedisian, AA; Dervin, SM; O'Dell, TJ; Voskuhl, RR; Ziehn, MO, 2012)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ziehn, MO1
Avedisian, AA1
Dervin, SM1
O'Dell, TJ1
Voskuhl, RR1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Double-Blind, Placebo Controlled Trial of Estriol Treatment in Women With Multiple Sclerosis: Effect on Cognition.[NCT01466114]Phase 264 participants (Anticipated)Interventional2011-10-31Recruiting
A Combination Trial of Copaxone Plus Estriol in RRMS[NCT00451204]Phase 2158 participants (Actual)Interventional2007-03-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Confirmed Relapse, Annualized Relapse Rate

A confirmed relapse was defined as new neurological symptoms or worsening of pre-existing symptoms, lasting at least 48 hours in a subject who had been neurologically stable or improving in the previous 30 days, accompanied by objective change in the neurological examination (worsening of 0.5 points on the EDSS or worsening by 1.0 or more points on the pyramidal, cerebellar, brainstem or visual functional system scores), not due to fatigue alone and not associated with fever or infection. (NCT00451204)
Timeframe: 12 months

Interventionrelapses per year (Mean)
Estriol Capsules Plus Copaxone Injections0.25
Placebo Capsules Plus Copaxone Injections0.48

Confirmed Relapse, Annualized Relapse Rate

A confirmed relapse was defined as new neurological symptoms or worsening of pre-existing symptoms, lasting at least 48 hours in a subject who had been neurologically stable or improving in the previous 30 days, accompanied by objective change in the neurological examination (worsening of 0.5 points on the EDSS or worsening by 1.0 or more points on the pyramidal, cerebellar, brainstem or visual functional system scores), not due to fatigue alone and not associated with fever or infection. (NCT00451204)
Timeframe: 24 months

Interventionrelapses per year (Mean)
Estriol Capsules Plus Copaxone Injections0.25
Placebo Capsules Plus Copaxone Injections0.37

Confirmed Relapse, Probability of First Relapse

(NCT00451204)
Timeframe: 24 months

Interventionprobability of relapse at 24 months (Mean)
Estriol Capsules Plus Copaxone Injections33.3
Placebo Capsules Plus Copaxone Injections42.9

Relapse Event, Annualized Relapse Rate

Met all criteria for relapse except not confirmed to have increase in EDSS by an independent examiner. (NCT00451204)
Timeframe: 12 months

Interventionrelapses per year (Mean)
Estriol Capsules Plus Copaxone Injections0.33
Placebo Capsules Plus Copaxone Injections0.61

Relapse Event, Annualized Relapse Rate

Met all criteria for relapse except not confirmed to have increase in EDSS by an independent examiner. (NCT00451204)
Timeframe: 24 months

Interventionrelapses per year (Mean)
Estriol Capsules Plus Copaxone Injections0.32
Placebo Capsules Plus Copaxone Injections0.46

Relapse Event, Probability of First Relapse Event

(NCT00451204)
Timeframe: 24 months

Interventionprobability of relapse event at 24 mo (Mean)
Estriol Capsules Plus Copaxone Injections40.5
Placebo Capsules Plus Copaxone Injections46.9

Other Studies

1 other study available for estriol and Demyelinating Diseases

ArticleYear
Estriol preserves synaptic transmission in the hippocampus during autoimmune demyelinating disease.
    Laboratory investigation; a journal of technical methods and pathology, 2012, Volume: 92, Issue:8

    Topics: Animals; CA1 Region, Hippocampal; Cell Adhesion Molecules, Neuronal; Demyelinating Diseases; Disks L

2012
Estriol preserves synaptic transmission in the hippocampus during autoimmune demyelinating disease.
    Laboratory investigation; a journal of technical methods and pathology, 2012, Volume: 92, Issue:8

    Topics: Animals; CA1 Region, Hippocampal; Cell Adhesion Molecules, Neuronal; Demyelinating Diseases; Disks L

2012
Estriol preserves synaptic transmission in the hippocampus during autoimmune demyelinating disease.
    Laboratory investigation; a journal of technical methods and pathology, 2012, Volume: 92, Issue:8

    Topics: Animals; CA1 Region, Hippocampal; Cell Adhesion Molecules, Neuronal; Demyelinating Diseases; Disks L

2012
Estriol preserves synaptic transmission in the hippocampus during autoimmune demyelinating disease.
    Laboratory investigation; a journal of technical methods and pathology, 2012, Volume: 92, Issue:8

    Topics: Animals; CA1 Region, Hippocampal; Cell Adhesion Molecules, Neuronal; Demyelinating Diseases; Disks L

2012