A Multicenter, non-comparative trial on the contraceptive efficacy, safety, and tolerability of LPRI-424 (dienogest 2 mg/ethinyl estradiol 0.02 mg) during 13 cycles
Sponsor: |
Chemo Research S.L |
Enrolling: |
Female Patients Only |
Study Length: |
13 Months |
Clinic Visits: |
9 |
IRB Number: |
AAAS7395 |
U.S. Govt. ID: |
NCT03945513 |
Contact: |
Carolyn Westhoff: 212-305-9368 / clw3@cumc.columbia.edu |
If you are a woman between the ages of 18 and 35, are pre-menopausal, sexually active and do NOT wish to become pregnant, you are invited to see if you may qualify for a research study. The purpose of this research study is to test the effectiveness of an investigational oral birth control pill. If you qualify, you will receive investigational study medication, study-related medical exams, and laboratory services at no charge. You may also be reimbursed for time, travel, and other expenses.
This study is closed
Investigator
Carolyn Westhoff, MD
Are you between 18 and 35 years of age? |
Yes |
No |
Are you currently sexually active with a male partner? |
Yes |
No |
Do you have a regular menstrual cycle? |
Yes |
No |