US Cycle Control and Blood Pressure Study

Completed · Phase 3 · Has a placebo group

Conditions studied: Contraception

In brief

Birth Control Patch Study

Key facts

Study ID

NCT00920985

Run by

Bayer

People needed

346

Starts

2009-06-01

Expected to finish

2010-09-01

Last updated by the study team

2015-10-09

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Female subject requesting contraception
• Age: 18 - 45 years (inclusive); smokers must not be older than 35 years at the time of informed consent
• Normal cervical smear not requiring further follow-up (a cervical smear has to be taken at screening visit or a normal result has to be documented within the previous 6 months)
• History of regular cyclic menstrual periods

You may not qualify if…

• Pregnancy or lactation
• Significant skin reaction to transdermal preparations or sensitivity to surgical / medical tape
• Any disease that may worsen under hormonal treatment (cardiovascular, liver, metabolic)
• Use of other contraceptive methods than study medication

Where it is running

• Study site — Chandler, Arizona, United States
• Study site — Glendale, Arizona, United States
• Study site — Phoenix, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Anaheim, California, United States
• Study site — San Diego, California, United States
• Study site — Clearwater, Florida, United States
• Study site — Daytona Beach, Florida, United States
• Study site — Lake Worth, Florida, United States
• Study site — Leesburg, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Atlanta, Georgia, United States
• Study site — Decatur, Georgia, United States
• Study site — Metairie, Louisiana, United States
• Study site — Kalamazoo, Michigan, United States
• Study site — St Louis, Missouri, United States
• Study site — Las Vegas, Nevada, United States
• Study site — New Brunswick, New Jersey, United States
• Study site — Winston-Salem, North Carolina, United States
• Study site — Cincinnati, Ohio, United States
• Study site — Philadelphia, Pennsylvania, United States
• Study site — Pittsburgh, Pennsylvania, United States
• Study site — Wexford, Pennsylvania, United States
• Study site — Columbia, South Carolina, United States
• Study site — Richmond, Virginia, United States

Full record on ClinicalTrials.gov

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