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Last Updated: April 16, 2024

CLINICAL TRIALS PROFILE FOR LYBREL


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All Clinical Trials for LYBREL

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00480532 ↗ A Study of Continuous Oral Contraceptives and Doxycycline Completed Oregon Health and Science University N/A 2007-05-01 The purpose of this study is to learn if the study drug, doxycycline, can decrease the amount of unplanned vaginal bleeding that women commonly experience when taking combined oral contraception (COC)- pills with estrogen and progestin - in a continuous fashion - no hormone-free week. The study drug, doxycycline, is an antibiotic used commonly for many conditions (i.e. acne, Chlamydia infections, pneumonia) and can be safely used on a daily basis. Doxycycline has been shown to decrease unplanned vaginal bleeding in progestin-only contraception but has not been studied in combined hormonal contraception.
NCT01297348 ↗ Study Of Lybrel In Relation To Venous Thromboembolism Completed Boston Collaborative Drug Surveillance Program 2007-07-01 Lybrel® is an oral contraceptive that delivers low doses of levonorgestrel and ethinyl estradiol (90 μg/20 μg). Lybrel is taken on a continuous basis without a placebo or pill-free interval to inhibit menstrual cycle bleeding by delivering a steady level of the 2 hormones for as long as the drug is used. Lybrel was marketed in the US in July of 2007. The objective of this database case-control study is to estimate the risk of idiopathic VTE (deep vein thrombosis and pulmonary embolism) in current users of Lybrel (ethinyl estradiol 20ug/levonorgestrel 90ug) compared to current users of other oral contraceptives containing 20μg of ethinyl estradiol.
NCT01297348 ↗ Study Of Lybrel In Relation To Venous Thromboembolism Completed Pfizer 2007-07-01 Lybrel® is an oral contraceptive that delivers low doses of levonorgestrel and ethinyl estradiol (90 μg/20 μg). Lybrel is taken on a continuous basis without a placebo or pill-free interval to inhibit menstrual cycle bleeding by delivering a steady level of the 2 hormones for as long as the drug is used. Lybrel was marketed in the US in July of 2007. The objective of this database case-control study is to estimate the risk of idiopathic VTE (deep vein thrombosis and pulmonary embolism) in current users of Lybrel (ethinyl estradiol 20ug/levonorgestrel 90ug) compared to current users of other oral contraceptives containing 20μg of ethinyl estradiol.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for LYBREL

Condition Name

Condition Name for LYBREL
Intervention Trials
Contraceptives, Oral 1
Pulmonary Embolism 1
Sinus Thrombosis, Intracranial 1
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Condition MeSH

Condition MeSH for LYBREL
Intervention Trials
Sinus Thrombosis, Intracranial 1
Pulmonary Embolism 1
Intracranial Thrombosis 1
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Clinical Trial Locations for LYBREL

Trials by Country

Trials by Country for LYBREL
Location Trials
United States 2
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Trials by US State

Trials by US State for LYBREL
Location Trials
Oregon 1
Hawaii 1
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Clinical Trial Progress for LYBREL

Clinical Trial Phase

Clinical Trial Phase for LYBREL
Clinical Trial Phase Trials
N/A 1
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Clinical Trial Status

Clinical Trial Status for LYBREL
Clinical Trial Phase Trials
Completed 2
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Clinical Trial Sponsors for LYBREL

Sponsor Name

Sponsor Name for LYBREL
Sponsor Trials
Oregon Health and Science University 1
Boston Collaborative Drug Surveillance Program 1
Pfizer 1
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Sponsor Type

Sponsor Type for LYBREL
Sponsor Trials
Other 2
Industry 1
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