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”

The purpose of the study is to use data from the Ingenix Research Database (a health care information database) to assess the risk of venous thromboembolism (blood clots), myocardial infarction (heart attacks), and stroke among women using the transdermal contraceptive system, ORTHO EVRA, compared with women using norgestimate-containing oral contraceptives with 35 mcg ethinyl estradiol.

Study Type: Observational

Study Design: Natural History, Longitudinal, Case Control, Retrospective Study

ORTHO EVRA (norelgestromin and ethinyl estradiol) is a newly developed transdermal contraceptive system (a "patch") available in the U.S. since April 2002. The study uses data from the Ingenix Research Database to assess the risk of venous thromboembolism [blood clots; pulmonary embolism (PE) and deep vein thrombosis (DVT)], acute heart attack, and stroke among women using the transdermal contraceptive system, ORTHO EVRA (norelgestromin and ethinyl estradiol), compared with women using norgestimate-containing oral contraceptives with 35 mcg ethinyl estradiol, during the period 4/1/2002 to 12/31/2004. The Ingenix Research Database is a United States health care claims database derived from comprehensive databases of UnitedHealth care. After obtaining IRB approval and a waiver of authorization, requests will be made for medical records for all patients whose claims sequence is possibly consistent with the occurrence of VTE (blood clots), AMI (heart attack), or stroke. A nested case control study will be conducted to estimate the relative risks of VTE (blood clots), AMI (heart attack, and stroke with special attention to duration of use of the last course of treatment before event onset. An additional case-control study will evaluate the effects of the risk estimates of missed cases in women on a professional sample of the contraceptive who do not have claims evidence of hormonal contraception and are non-pregnant childbearing aged.

Transdermal patch containing 6 mg norelgestromin and 0.75 mg ethinyl estradiol worn for 1 week and replaced for 3 consecutive weeks; 4th week is patch-free. Norgestimate-containing oral contraceptives with 35 mcg ethinyl estradiol taken 21 consecutive days, then no pill or a drug-free pill 7 days.

Inclusion Criteria:

• Users of Ortho Evra or norgestimate-containing oral contraceptives with 35 mcg ethinyl estradiol between April 1, 2002 and December 31, 2004, who are identified in the Ingenix Research Database
• Have complete medical coverage and pharmacy benefits
• Enrollment data showing sex of female

Exclusion Criteria:

• Have a claim associated with physician services for any of the following: malignancy other than non-melanoma skin cancer
• Coagulation defects, history of venous thrombus/embolism, or long-term anticoagulant use
• Chronic inflammatory disease

Gender Eligibility for this Clinical Trial: Female

Minimum Age for this Clinical Trial: 15 Years

Maximum Age for this Clinical Trial: 44 Years

Are Healthy Volunteers Accepted for this Clinical Trial?: Accepts Healthy Volunteers

Lead Sponsor: Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

Overall Clinical Trial Officials and Contacts

Johnson & Johnson Pharmaceutical Research and Development, L.L.C. Clinical Trial Study Director Johnson & Johnson Pharmaceutical Research & Development, L.L.C.  

Information obtained from ClinicalTrials.gov on October 07, 2008

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00377988

Study ID Number: CR012022

ClinicalTrials.gov Identifier: NCT00377988

Health Authority: United States: Institutional Review Board

Myocardial infarction, stroke, and venous thromboembolism among transdermal contraceptive system users