Results 161 to 170 of about 2,739 (201)

Changes in the vaginal microbiota in ewes after insertion of intravaginal sponges at different stages of the oestrous cycle

open access: yesLivestock Science, 2018
The aims of this study were to determine if the ewe’ vaginal bacterial load differs according to the stage of the oestrous cycle; and thus, if the stage of the oestrous cycle when intravaginal sponges (IS) used for oestrous synchronisation are inserted
Maria A Fiorentino, Rodolfo Ungerfeld
exaly   +2 more sources

The Effectiveness of Using Antibiotic with Intravaginal Sponge and Duration of Sponge Treatments on the Vaginal Flora and Fertility in Anestrous Ewes

open access: yes, 2008
The aim of this study was to compare effectiveness of antibiotic administration to intravaginal sponge before sponge insertion and investigate duration of sponge treatment for determining changes in the vaginal bacterial flora and fertility parameters.
Ozyurtlu, Nihat   +2 more
openaire   +2 more sources

Toxic Shock Syndrome and the Vaginal Contraceptive Sponge

Obstetrical & Gynecological Survey, 1986
Thirteen confirmed cases of toxic shock syndrome temporally related to use of the vaginal contraceptive sponge have been reported. The observed risk of toxic shock syndrome in sponge users may be elevated above estimated background rates, but this risk remains very low.
G, Faich   +4 more
  +5 more sources

Vaginal mucus from ewes treated with progestogen sponges affects quality of ram spermatozoa

open access: yesTheriogenology, 2016
The use of intravaginal sponges (IS) to synchronize estrous onset in ewes provokes vaginitis, an increase in the vaginal bacterial load, and growth of bacterial species that are not present during spontaneous estrous behavior.
Maria A Fiorentino, Rodolfo Ungerfeld
exaly   +2 more sources

Spermicides, HIV, and the Vaginal Sponge

JAMA: The Journal of the American Medical Association, 1992
Despite the current epidemic of sexually transmitted human immunodeficiency virus (HIV) infection and other sexually transmitted diseases (STDs), prevention measures known to be effective are underutilized. Most prevention guidelines have appropriately emphasized abstinence, monogamy between uninfected partners, or condom use.
K M, Stone, H B, Peterson
openaire   +3 more sources

Food and Drug Administration Approves Vaginal Sponge

Family Planning Perspectives, 1983
On April 1 1983 the US Food and Drug Administration (FDA) approved a disposable vaginal sponge of soft polyurethane foam saturated with 1 gm of nonoxynol-9 as a nonprescription contraceptive offering 2 improvements over products already available: ability to leave in place up to 24 hours and no need for additional application of spermicide for ...
D, Kafka, R B, Gold
openaire   +2 more sources

Metronidazole-containing vaginal sponges for the treatment of bacterial vaginosis

Advances in Contraception, 1986
Currently, there is no FDA approved treatment for bacterial vaginosis (BV), although various oral dosages of metronidazole are used to treat this condition. A vaginal therapeutic sponge (VLI Corporation) that releases metronidazole over a 24 h use period has been developed for the treatment of BV. Each sponge contains 250 mg of metronidazole.
W E, Brenner, J R, Dingfelder
openaire   +2 more sources

A System-Wide Initiative to Prevent Retained Vaginal Sponges

MCN: The American Journal of Maternal/Child Nursing, 2011
As any perinatal nurse knows, retained vaginal sponges are an obstetrical and postpartum patient safety problem. As surgical sponge counts are not routine in some obstetrical units for vaginal births, our healthcare system chose to institute a rigorous process to eliminate retained sponges in all vaginal births.
Brenda A, Chagolla   +3 more
openaire   +2 more sources

Worldwide method effectiveness of the Today® vaginal contraceptive sponge

Advances in Contraception, 1985
The Today vaginal contraceptive sponge is made of polyurethane and contains 1 gram of the spermicide nonoxynol-9. Following preclinical and phase I and II clinical trials, extensive worldwide phase III trials were conducted. These multiclinic trials were conducted according to a common protocol with regularly scheduled follow-up visits and examinations.
D A, McClure, D A, Edelman
openaire   +2 more sources

Home - About - Disclaimer - Privacy