drugset / Trial / NCT01815138

Co-administration of Low Dose hCG at the Time of GnRH Agonist Trigger or 35 Hours Later for the Prevention of OHSS

NCT01815138

Phase 4 Completed 89 enrolled UConn Health Merck Sharp & Dohme LLC · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This a prospective randomized double blind study involving patients at high risk of OHSS development with peak serum E2 levels \< 4,000 pg/ml comparing the ongoing pregnancy rates in patients who receive adjuvant hCG 1,000 IU at the time of GnRH agonist trigger or adjuvant hCG 1,500 IU 35 hours after GnRH agonist trigger.

Timeline

Start
2013-03
Primary completion
2015-12
Completion
2016-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator human chorionic gonadotropin Protein / enzyme biologic 1000 iu
Comparator human chorionic gonadotropin Protein / enzyme biologic 1500 iu