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Follicular Challenge Test to Predict Response to GnRH Agonist Triggering

Follicular Challenge Test to Predict Response to GnRH Agonist Triggering

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04973969
Enrollment
100
Registered
2021-07-22
Start date
2021-01-01
Completion date
2022-04-30
Last updated
2021-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility, Female

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.

Interventions

diagnosis of predictio value

Sponsors

Assaf-Harofeh Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 41 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
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

Countries

Israel

Contacts

Primary ContactSarit Avraham, Dr
sarita@shamir.gov.il00972522371126

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026