Assisted Reproduction
Conditions
Brief summary
Efficacy of the use of GnRH antagonist in treatment of those who develop early-onset severe ovarian hyperstimulation syndrome and had cancelled embryo transfer
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
* Women who develop early-onset severe ovarian hyperstimulation syndrome after controlled ovarian stimulation using long GnRH agonist protocol and hCG for triggering ovulation.
Exclusion criteria
* Women on short or antagonist protocols. * Women who received GnRH agonist for triggering ovulation. * Women who had embryo transfer.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of women who needed culdocentesis or paracentesis of the ascitic fluid | within 2 weeks of onset |
Secondary
| Measure | Time frame |
|---|---|
| Number of women who needed hospitalization | within 2 weeks of onset of symptoms |
| Time to regression of nausea/vomiting | within 2 weeks of onset of symptoms |
| Time to regression of large ovarian size | within 4 weeks of onset of symptoms |