Clinical trial

A Postmarketing Study of the Risk of Venous Thromboembolism (Blood Clots)…

NCT00377988 · Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry · Completed

Key facts

NCT number NCT00377988
Title A Postmarketing Study of the Risk of Venous Thromboembolism (Blood Clots), Myocardial Infarction (Heart Attacks), and Stroke Among Women Using ORTHO EVRA (Norelgestromin and Ethinyl Estradiol Contraceptive Patch) Compared With Women Who Take Oral Contraceptives for Birth Control
Official title The Risk of Venous Thromboembolism, Myocardial Infarction, and Ischemic Stroke Among Women Using the Transdermal Contraceptive System Compared With Women Using Norgestimate-containing Oral Contraceptives With 35 mcg Ethinyl Estradiol
Lead sponsor Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry
Status Completed
Study type Observational
Conditions Contraception, Female Contraception
Intervention type Drug
Interventions Transdermal Contraceptive System, Norgestimate-containing oral contraceptives with EE
Enrollment 423
Start date Apr 1, 2002
Primary completion Oct 1, 2008
Completion Oct 1, 2008
First posted Sep 19, 2006
Last update posted Jul 19, 2016

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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