A Phase I study of the functional performance, safety and acceptability of the BufferGel® Duet™☆☆☆
To access this article, please choose from the options below
☆ Support for this project was provided by CONRAD, Eastern Virginia Medical School, under a Cooperative Agreement with the United States Agency for International Development (USAID). The study product was supplied by ReProtect, Baltimore, MD.
☆☆ The views expressed by the authors do not necessarily reflect the views of USAID.
PII: S0010-7824(07)00455-6
doi:10.1016/j.contraception.2007.10.003
© 2008 Elsevier Inc. All rights reserved.
