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Clinical Trial Summary

The purpose of this study is to prove that luteal phase supplementation with recombinant LH can solve the luteal phase deficiency after Gnrh agonist oocytes triggering in women at risk of OHSS


Clinical Trial Description

The investigators enrolled patients, undergoing controlled ovarian stimulation for an IVF/ICSI cycles, who on the day of oocytes triggering were at risk of OHSS. These patients had an estradiol > 4000 pg/ml and more than 24 follicles with a diameter greater than 12 mm. The investigators used 0,2 mg of triptorelin for the oocytes triggering and supplemented the luteal phase with recombinant LH at a dose of 75 UI twice/day for 10 days and vaginal gel progesterone and oral oestradiol for 14 days The investigators measured bhCG at 14 days from the pick up. In case of positive bhCG we have defined the IVF/ICSI outcome: Pregnancy Rate and Implantation Rate. ;


Study Design


Related Conditions & MeSH terms

  • Ovarian Hyperstimulation Syndrome

NCT number NCT02200952
Study type Observational [Patient Registry]
Source San Carlo Public Hospital, Potenza, Italy
Contact
Status Completed
Phase
Start date June 30, 2013
Completion date June 30, 2014

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