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Follicular Challenge Test to Predict Response to GnRH Agonist Triggering

Not Applicable
Conditions
Infertility, Female
Registration Number
NCT04973969
Lead Sponsor
Assaf-Harofeh Medical Center
Brief Summary

GnRH agonist triggering is used during ART in order to reduce the risk of OHSS. Some studies described that in up to 5% of the cycles triggered with GnRH agonist, a lack of respone or suboptimal response was displayed.

The investigators aim to asses the possibility to predict the respone to ovulation triggering by the response to decapeptyl in the follicular phase of the same cycle.

Detailed Description

The investigators will use Decapeptyl on day 2 of menstruation followed by antagonist protocol.

Hormonal proflie including E2, P, LH, FSH will be measured. LH surge and the rest of the hormonal profile will be compared to day after ovulation triggering.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
100
Inclusion Criteria
  • patients that undergo fertility preservation

    • patients planned to freeze embryos due to PGT or surrogacy --patients at high risk for OHSS
Exclusion Criteria
  • Poor ovarian response
  • known hypothalamic- pituitary dysfunction

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
The response to GnRH triggeringOne treatment cycle (each cycle is 28 days) for each participant (up to 28 days).

LH levels 10-12 hours after decapeptyl trigger, number of mature oocytes

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Shamir medical center

🇮🇱

Tzrifin, Israel

Shamir medical center
🇮🇱Tzrifin, Israel
Sarit Avraham, Dr
Contact

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