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Last Updated: November 11, 2024

CLINICAL TRIALS PROFILE FOR ESTROGENS, CONJUGATED SYNTHETIC A


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All Clinical Trials for Estrogens, Conjugated Synthetic A

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00006133 ↗ Randomized Study of Oral Contraceptives or Hormone Replacement Therapy in Women With Systemic Lupus Erythematosus Completed University of Alabama at Birmingham N/A 2000-06-01 OBJECTIVES: I. Determine the effect of oral contraceptives containing low-dose synthetic estrogens and progestins on disease activity in premenopausal women with inactive, stable, or moderate systemic lupus erythematosus (SLE). II. Determine the effect of hormone replacement therapy with conjugated estrogens and progestins on disease activity in postmenopausal women with inactive, stable, or moderate SLE.
NCT00006133 ↗ Randomized Study of Oral Contraceptives or Hormone Replacement Therapy in Women With Systemic Lupus Erythematosus Completed National Center for Research Resources (NCRR) N/A 2000-06-01 OBJECTIVES: I. Determine the effect of oral contraceptives containing low-dose synthetic estrogens and progestins on disease activity in premenopausal women with inactive, stable, or moderate systemic lupus erythematosus (SLE). II. Determine the effect of hormone replacement therapy with conjugated estrogens and progestins on disease activity in postmenopausal women with inactive, stable, or moderate SLE.
NCT00196378 ↗ A Clinical Trial to Evaluate the Safety and Efficacy of Enjuvia 0.3 mg for the Treatment of Vulvovaginal Atrophy Completed Duramed Research Phase 3 2004-11-01 This is a two-arm, randomized, double-blind, parallel-group, placebo-controlled study to evaluate the efficacy of Enjuvia 0.3 mg tablets for the treatment of moderate to severe symptoms of vulvovaginal atrophy in postmenopausal women with or without a hysterectomy and/or oophorectomy.
NCT00272935 ↗ A Clinical Trial to Demonstrate the Efficacy and Safety of Cenestin 0.3 mg for the Treatment of Hot Flashes Completed Duramed Research Phase 3 2005-12-01 This is a randomized, double-blind study to compare the efficacy and safety of daily doses of Cenestin 0.3 mg tablets to placebo in reducing the frequency and severity of moderate to severe hot flashes in postmenopausal women.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Estrogens, Conjugated Synthetic A

Condition Name

Condition Name for Estrogens, Conjugated Synthetic A
Intervention Trials
Menopause 2
Schizoaffective Disorder 1
Schizophrenia 1
Schizophreniform Disorder(Not in Manic Phase) 1
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Condition MeSH

Condition MeSH for Estrogens, Conjugated Synthetic A
Intervention Trials
Atrophy 2
Psychotic Disorders 1
Disease 1
Hot Flashes 1
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Clinical Trial Locations for Estrogens, Conjugated Synthetic A

Trials by Country

Trials by Country for Estrogens, Conjugated Synthetic A
Location Trials
United States 98
Australia 1
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Trials by US State

Trials by US State for Estrogens, Conjugated Synthetic A
Location Trials
Texas 5
Pennsylvania 5
California 5
Oregon 4
Ohio 4
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Clinical Trial Progress for Estrogens, Conjugated Synthetic A

Clinical Trial Phase

Clinical Trial Phase for Estrogens, Conjugated Synthetic A
Clinical Trial Phase Trials
Phase 4 1
Phase 3 3
Phase 2 1
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Clinical Trial Status

Clinical Trial Status for Estrogens, Conjugated Synthetic A
Clinical Trial Phase Trials
Completed 6
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Clinical Trial Sponsors for Estrogens, Conjugated Synthetic A

Sponsor Name

Sponsor Name for Estrogens, Conjugated Synthetic A
Sponsor Trials
Duramed Research 4
The Alfred 1
University of Alabama at Birmingham 1
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Sponsor Type

Sponsor Type for Estrogens, Conjugated Synthetic A
Sponsor Trials
Industry 4
Other 3
NIH 1
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