Contraception, Female Contraception
Conditions
Keywords
contraception, transdermal contraception, hormonal, steroidal contraception, ethinyl estradiol, progesterone
Brief summary
The purpose of the study is to evaluate the contraceptive efficacy, safety, cycle control, and compliance with the transdermal contraceptive system.
Detailed description
This is an open-label, multicenter, global study to evaluate the contraceptive efficacy, cycle control, safety, compliance and subject satisfaction of the transdermal contraceptive system. Sixteen hundred healthy women will wear the contraceptive patch for either 6 or 13 cycles. The first 530 subjects will wear the patch for 13 cycles, and all subsequent subjects will wear the patch for 6 cycles. At admission Visit 1, study drug (plus 3 reserve patches) and diary cards are dispensed for Cycle 1; first patch application will be on the first day of menses. Study drug and diary cards are dispensed on day 28 of Cycle 1 (Visit 2) for Cycles 2 and 3, on day 28 of Cycle 3 (Visit 3) for Cycles 4 to 6, on day 28 of Cycle 6 (Visit 4) for Cycles 7 to 9, and on day 28 of Cycle 9 (Visit 5) for Cycles10 to13. At each of these visits, diary cards and empty medication packages are collected. Final study visits are on day 28 of Cycles 6 and 13. Diary card information is used to record compliance and bleeding information (to assess cycle control). Contraceptive efficacy is assessed by means of the Pearl Index and life table analysis (gross cumulative probability of pregnancy). Safety evaluations are based on adverse events, which are collected throughout the study, and changes in gynecologic examinations, vital signs, and laboratory results from admission to final visit. Each transdermal contraceptive patch, containing 6 mg NGM and 0.75 mg EE, and delivering 250 ug 17-dNGM and 25 ug EE over 24 hours for 7 days, is worn for 1 week and replaced for 3 consecutive weeks. The fourth week is patch-free. The patch can be worn on: upper arm or torso, buttock, or abdomen.
Interventions
Sponsors
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* Healthy women with regular menstrual cycles * sexually active and at risk of pregnancy * nonpregnant * acceptable body mass index (BMI) * last term pregnancy at least 42 days prior, nonlactating, with 1 normal menstrual cycle since * sitting BP\<140mmHg/\<90mmHg * 1 normal menstrual cycle since removal of IUD or norplant * agreement to use study drug for contraception for up to 13 cycles, except when backup contraception is required for disease protection or patch detachment * agree not to use other systemic steroid medication
Exclusion criteria
* Presence, history, hereditary predisposition or risk of deep vein thrombophlebitis or thromboembolic disorders * cerebral vascular or coronary artery disease, hypertension, or severe migraines * liver tumor resulting from estrogen-containing products * diabetes mellitus * cholestatic jaundice, liver or renal disease * abnormal PAP smear * thyroid disorder * dermal hypersensitivity * carcinoma of breast, endometrium or other estrogen-dependent neoplasia * substance abuse * received experimental drug within prior 30 days * smoking women over 35 years of age.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Contraceptive efficacy is assessed with the Pearl Index and life table analysis (gross cumulative probability of pregnancy). Safety is evaluated throughout the study. | — |
Secondary
| Measure | Time frame |
|---|---|
| Cycle control and compliance are assessed with diary cards containing bleeding information and dosing information. | — |
Outcome results
None listed