 | ||||||
 |  | |||||
 | ||||||
  | ||||||
Birth Control Study:Study: Oral Birth Control Pill Study Description: A multicenter, open label study to evaluate the efficacy and safety of a combination oral contraceptive regimen for the prevention of pregnancy in women Entry Criteria: Must be on Birth Control pills for at least 3 months continuously.
Study Duration: Participant will have 7 office visits over a 12 month period Compensation: The Subject will receive all study related office visits, laboratory testing, and medication at no cost. Additionally the subject may be compensated for time and travel expenses up to $450. Contact Nina Zaniefski: (727) 724-9730 ninaz@xxresearch.com
Birth Control Study:Study: Oral Birth Control #2 Description: A multinational, multicenter, randomized, open label study to evaluate the impact of a 91 day extended cycle oral contraceptive regimen, compared to two 28-day standard oral contraceptive regimens on hemostatic parameters in healthy women Entry Criteria:
Study Duration: Participant will have 4 office visits over a 8 month period Compensation: The Subject will receive all study related office visits, laboratory testing, and medication at no cost. Additionally the subject may be compensated for time and travel expenses up to $100. Contact Nina Zaniefski: (727) 724-9730 ninaz@xxresearch.com |  | |||||
 | ||||||
 | ||||||
 | ||||||
 | ||||||
 | ||||||
 | ||||||
 |
||||||
 | ||||||
| | | | | | |
 | ||
| | |
| | |