Compliance with Yaz Flex supported by the CADDY
Research type
Research Study
Full title
A multicenter, open-label, randomized, controlled, two-arm study to assess compliance with daily tablet intake of women on treatment with the oral contraceptive SH T00186D/BAY 86-5300 (0.02 mg ethinyl estradiol as betadex clathrate and 3 mg drospirenone) in a flexible extended regimen supported by a dispenser (CADDY) with a reminder function over 12 months
IRAS ID
56695
Contact name
Nell Wyatt
Sponsor organisation
Bayer HealthCare AG, c/o Bayer plc
Eudract number
2010-019902-17
ISRCTN Number
N/A
Research summary
The objective of the study is to evaluate the effect of the dispenseris buzzer function on compliance with daily tablet intake of an ethinyl estradiol (EE) drispirenone (DRSP) containing oral contraceptive (OC) in a flexible extended regimen when administered for approximately 12 months to healthy female volunteers who request contraception.
REC name
South Central - Oxford B Research Ethics Committee
REC reference
10/H0605/68
Date of REC Opinion
17 Dec 2010
REC opinion
Further Information Favourable Opinion