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Progesterone vaginal ring: Results of a three-country acceptability study
Author(s) -
Saumya RamaRao,
Heather Clark,
Deepa Rajamani,
Salisu Ishaku,
Babacar Mané,
Francis Obare,
Harriet Birungi,
Nafissatou Diop,
Wilson Liambila,
Fatou Mbow,
ChiChi Undie,
Godwin Unumeri,
John Townsend
Publication year - 2015
Language(s) - English
Resource type - Reports
DOI - 10.31899/rh9.1063
Subject(s) - vaginal ring , latin americans , breastfeeding , developing country , medicine , family planning , population , family medicine , clinical trial , economic growth , gynecology , environmental health , business , political science , pediatrics , research methodology , pathology , law , economics
The progesterone vaginal ring (PVR) is a contraceptive designed specifically for use by breastfeeding women in the first year postpartum. The PVR is inserted in the vagina 30-90 days postpartum for continuous use for up to 3 months and replaced with a new ring if breastfeeding is continued and extended contraception is desired. Women can use four rings successively for up to one year. The progesterone vaginal ring functions by diffusing a continuous flow of progesterone through the vaginal walls--approximately 10 mg per day--which then enters the bloodstream and regulates the woman’s fertility by suppressing ovulation. Clinical trials have proven the PVR to be a safe and effective contraceptive; furthermore it is currently registered in eight countries in Latin America. The PVR has also been included in the 2015 WHO Essential Medicines List and the Medical Eligibility Criteria guidance. This study was part of a series of activities that assess the feasibility of and preparation for introduction of the PVR into Kenya Nigeria and Senegal. (excerpt)

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