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From the Wires
Reproductive Partners Participates in New IVF Progesterone Delivery System Study
By: PR Newswire
Jan. 12, 2009 01:20 PM
The study compares an FDA-approved vaginal progesterone, Endometrin, with a new formulation which is administered subcutaneously, similar to the relatively painless fertility drug injections. Patients will be randomized to receive either the vaginal or subcutaneous progesterone until the pregnancy test and then until about 10 weeks of pregnancy. In case of unacceptable side effects the patient will be offered an alternative medication. Side effects are usually local reactions and mild. Benefits to patients include free progesterone medications as well as a Participating patients will be IVF candidates, including those undergoing ICSI, Blastocyst and PGD, who are age 18-42 who have had less than three prior IVF cycles and an FSH less than 15IU/L and estradiol less than 80 pg/mL. Other exclusion criteria exist. For more information, please visit www.reproductivepartners.com or call Reproductive Partners Medical Group at (877) 273-7763. SOURCE Reproductive Partners Medical Group
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