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https://www.readbyqxmd.com/read/25100106/a-randomized-controlled-trial-comparing-the-efficacy-and-safety-of-aqueous-subcutaneous-progesterone-with-vaginal-progesterone-for-luteal-phase-support-of-in-vitro-fertilization
#1
RANDOMIZED CONTROLLED TRIAL
Valerie L Baker, Christopher A Jones, Kevin Doody, Russell Foulk, Bill Yee, G David Adamson, Barbara Cometti, Gary DeVane, Gary Hubert, Silvia Trevisan, Fred Hoehler, Clarence Jones, Michael Soules
STUDY QUESTION: Is the ongoing pregnancy rate with a new aqueous formulation of subcutaneous progesterone (Prolutex(®)) non-inferior to vaginal progesterone (Endometrin(®)) when used for luteal phase support of in vitro fertilization? SUMMARY ANSWER: In the per-protocol (PP) population, the ongoing pregnancy rates per oocyte retrieval at 12 weeks of gestation were comparable between Prolutex and Endometrin (41.6 versus 44.4%), with a difference between groups of -2...
October 10, 2014: Human Reproduction
https://www.readbyqxmd.com/read/24140033/subcutaneous-progesterone-versus-vaginal-progesterone-gel-for-luteal-phase-support-in-in%C3%A2-vitro-fertilization-a-noninferiority-randomized-controlled-study
#2
RANDOMIZED CONTROLLED TRIAL
Gillian Lockwood, Georg Griesinger, Barbara Cometti
OBJECTIVE: To compare the safety, efficacy, and tolerability of subcutaneous progesterone (Prolutex, 25 mg; IBSA Institut Biochimique SA) with vaginal progesterone gel (Crinone, 8%; Merck Serono) for luteal phase support (LPS) in assisted reproduction technologies (ART) patients. DESIGN: Prospective, open-label, randomized, controlled, parallel-group, multicenter, two-arm, noninferiority study. SETTING: Thirteen European fertility clinics...
January 2014: Fertility and Sterility
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