Overview
A Study of Use of Ella®, an Emergency Contraceptive, Under Simulated OTC Conditions
Status:
Completed
Completed
Trial end date:
2018-06-14
2018-06-14
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
This study is designed to assess whether consumers select and use ella® (ulipristal acetate 30mg), an emergency contraceptive, in a manner consistent with the OTC package directions in an OTC-like setting.Phase:
Phase 3Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
HRA PharmaTreatments:
Contraceptives, Postcoital
Ulipristal acetate
Criteria
Inclusion Criteria:- Women who are self-pay or who are willing to be self-pay for the purposes of the study
and who present for emergency contraception only for their own use
Exclusion Criteria:
- Cannot read, speak and understand English
- Cannot see well enough to read information on the label