Design Data from two randomized phase III trials (07EU/Prg06 and 07USA/Prg05)
efficacy and safety of aqueous subcutaneous progesterone with vaginal progesterone for luteal phase support of in vitro fertilization
) and intramuscular (i
A randomized trial comparing the endometrial effects of daily subcutaneous administration of 25mg and 50 mg of progesterone in aqueous preparation Fertil Steril , 100 ( 2013 ) , pp
1093/humrep/deu194
galen os
Background: The requirement of luteal phase support in in vitro fertilization cycles is necessary
A randomized, controlled trial comparing the efficacy and safety of aqueous subcutaneous progesterone with vaginal progesterone for luteal phase
Each site was asked to enrol 100 patients with equal numbers assigned to Prolutex and Endometrin
For both doses, the P preparation was reconstituted by dissolving 50 mg lyophilized powder in 1 mL injectable aqueous solution; 1