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Last Updated: October 14, 2024

CLINICAL TRIALS PROFILE FOR DROSPIRENONE; ESTRADIOL


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All Clinical Trials for Drospirenone; Estradiol

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00102141 ↗ Effect of Angeliq on Blood Pressure (BP) in Postmenopausal Hypertensive Women Completed Bayer Phase 3 2004-04-01 The objective of the study is to evaluate the effects of Angeliq on BP over a period of 8 weeks in postmenopausal women who may benefit from hormone replacement therapy (HRT) for the relief of vasomotor symptoms and who have hypertension.
NCT00356447 ↗ Safety/Efficacy Study of Drospirenone/Estradiol to Treat Postmenopausal Chinese Women With Vasomotor Symptoms. Completed Bayer Phase 3 2006-05-01 The study evaluates in Chinese post-menopausal women the combination of drospirenone 2 mg and estradiol 1 mg for the treatment of climacteric symptoms, such as hot flushes (vasomotor symptoms) and uro-genital complaints.
NCT00413062 ↗ Efficacy and Safety Study of the Combined Oral Contraceptive NOMAC-E2 Compared to a COC Containing DRSP/EE (292002)(P05722) Completed Merck Sharp & Dohme Corp. Phase 3 2006-06-01 The primary purpose of this study is to assess contraceptive efficacy, vaginal bleeding patterns (cycle control), general safety and acceptability of the nomegestrol acetate-estradiol (NOMAC-E2) combined oral contraceptive (COC) in a large group of women aged 18-50 years.
NCT00420342 ↗ Effects of Angeliq and Prempro on Blood Pressure and Sodium Sensitivity in Postmenopausal Women With Prehypertension Completed Bayer Phase 2 2007-01-01 The main purpose of this study is to compare the effects of treatment of two different formulations of Angeliq® and Prempro on blood pressure in post-menopausal women with prehypertension.
NCT00446199 ↗ Low-dose Hormone Therapy for Relief of Vasomotor Symptoms Completed Bayer Phase 3 2007-03-01 The purpose of this study is to determine the lowest effective dose of the study drug for the relief of moderate to severe vasomotor symptoms in postmenopausal women for 12 weeks.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Drospirenone; Estradiol

Condition Name

Condition Name for Drospirenone; Estradiol
Intervention Trials
Contraception 11
Polycystic Ovary Syndrome 5
Premenstrual Syndrome 4
Healthy 4
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Condition MeSH

Condition MeSH for Drospirenone; Estradiol
Intervention Trials
Syndrome 6
Polycystic Ovary Syndrome 5
Endometriosis 4
Premenstrual Syndrome 4
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Clinical Trial Locations for Drospirenone; Estradiol

Trials by Country

Trials by Country for Drospirenone; Estradiol
Location Trials
United States 138
China 25
Germany 23
Austria 9
United Kingdom 6
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Trials by US State

Trials by US State for Drospirenone; Estradiol
Location Trials
Pennsylvania 8
Florida 8
California 8
Texas 7
Arizona 6
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Clinical Trial Progress for Drospirenone; Estradiol

Clinical Trial Phase

Clinical Trial Phase for Drospirenone; Estradiol
Clinical Trial Phase Trials
Phase 4 12
Phase 3 21
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for Drospirenone; Estradiol
Clinical Trial Phase Trials
Completed 33
Unknown status 7
Recruiting 2
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Clinical Trial Sponsors for Drospirenone; Estradiol

Sponsor Name

Sponsor Name for Drospirenone; Estradiol
Sponsor Trials
Bayer 22
Massachusetts General Hospital 3
Merck Sharp & Dohme Corp. 3
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Sponsor Type

Sponsor Type for Drospirenone; Estradiol
Sponsor Trials
Industry 34
Other 24
NIH 1
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