Status:
COMPLETED
Evaluation of Pharmacodynamic Effects on Ovulation and Cycle Control
Lead Sponsor:
Agile Therapeutics
Conditions:
Ovulation Suppression
Eligibility:
FEMALE
18-45 years
Phase:
PHASE2
Brief Summary
Evaluate the adequacy of ovulation suppression, cycle control, and safety of three transdermal contraceptive delivery systems (TCDSs).
Detailed Description
The primary objective was to evaluate the adequacy of ovulation suppression, cycle control, and safety of three transdermal contraceptive delivery systems (TCDSs) containing 2 different doses of levon...
Eligibility Criteria
Inclusion
- Healthy adult women, ages 18-45.
- Cycles with a usual duration between 21 and 35 days and an individual variation of +/ 3 days.
- Normotensive (blood pressure \< 140/90 mm Hg at rest) at screening and randomization visits (Visits 1 and 2).
- Willing to use a non-hormonal method of contraception for the entire duration of the study, or
- Have already undergone previous bilateral tubal ligation OR vasectomized partner OR not at risk of pregnancy.
- Willing to refrain from excessive use of alcohol during the entire duration of the study.
- Willing to give informed consent to participate in the study.
Exclusion
- History of significant medical illness or seizures.
- Positive hepatitis B or C antibody or positive human immunodeficiency virus (HIV) antibody.
- Known or suspected pregnancy.
- A recent abnormal cervical smear - low-grade squamous intraepithelial lesion (SIL) or higher in the Bethesda System - which has not been resolved or treated.
- Any disorder that contraindicates the use of contraceptive steroids i.e., history of heart attack and stroke, blood clots in the legs, lungs or eyes, history of blood clots in the deep veins of the legs, known or suspected breast cancer, hepatitis or yellowing of the whites of the eyes or the skin (jaundice) during pregnancy or during previous use of hormonal contraceptives, headaches with neurological symptoms, disease of heart valves with complications.
- Uncontrolled thyroid disorder.
- History of or existing thromboembolic disorder, vascular disease, cerebral vascular, or coronary artery disease.
- Undiagnosed abnormal genital bleeding.
- Known or suspected breast carcinoma, endometrial carcinoma, or estrogen-dependent neoplasia.
- History or presence of dermal hypersensitivity in response to topical application.
- Use of an injectable hormonal contraceptive (e.g. Depo-Provera®) within 6 months prior to Day 1.
- Use of a contraceptive implant (e.g. Implanon® or Jadelle®) or hormone-medicated intrauterine device within 2 months (60 days) prior to Day 1.
- Use of OCs or other sex steroid hormones within 60 days prior to Day 1.
- Women who are breast-feeding or are within 2 months of stopping breast-feeding.
- Status post-partum or post-abortion within a period of 2 months prior to Day 1.
- Chronic use of any medication that might interfere with the metabolism of hormone contraceptives (e.g., rifampin, barbiturates, phenytoin, primidone, topiramate, carbamazepine, phenylbutazone, ritonavir, modafinil, St John's Wort etc.) or use within the past 3 months prior to Day 1.
- Administration of investigational drug within 30 days prior to Day 1.
- A history (within prior 12 months) of drug or alcohol abuse.
- Women who smoke more than 4-5 cigarettes daily.
- History of skin sensitivity to adhesives.
- Use of over-the-counter medications or herbals that might interfere with the metabolism of hormone contraceptives within 3 days prior to wearing the first patch.
Key Trial Info
Start Date :
September 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2008
Estimated Enrollment :
123 Patients enrolled
Trial Details
Trial ID
NCT01250210
Start Date
September 1 2007
End Date
February 1 2008
Last Update
July 5 2018
Active Locations (11)
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1
Tucson, Arizona, United States, 85712
2
San Diego, California, United States, 92108
3
Denver, Colorado, United States, 80218
4
Pembroke Pines, Florida, United States, 33026