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Double Trigger in Patients With Low Number of Oocytes Retrieved Per Number of Preovulatory Follicles

R

Riyadh Fertility and Reproductive Health center

Status and phase

Unknown
Phase 2

Conditions

Infertility, Female

Treatments

Drug: HCG trigger
Drug: Double trigger

Study type

Interventional

Funder types

Other

Identifiers

NCT04407065
Double trigger/more oocytes

Details and patient eligibility

About

The aim of this randomized controlled trial is to determine whether co-administration of GnRH agonist and hCG for final oocyte maturation ( 40 and 34 h prior to oocyte retrieval , respectively) can increase the oocytes yield in patients with history of poor oocytes yield, despite normal response to COH, due to low (<50%) number of oocytes retrieved per number of follicles > 14 mm in diameter on day of hCG administration

Enrollment

56 estimated patients

Sex

Female

Ages

18 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with history of poor oocytes yield in previous IVF attempt, despite normal response to COH, due to low (<50%) number of oocytes retrieved per number of follicles > 14 mm in diameter on day of hCG administration
  • Patients with 6 to 15 mature follicles on the day oocyte trigger in the current IVF-ET attempt

Exclusion criteria

  • Endometriosis
  • PCOS

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

56 participants in 2 patient groups

Double trigger
Experimental group
Description:
GnRH-agonist and HCG are used to trigger ovulation
Treatment:
Drug: Double trigger
HCG
Active Comparator group
Description:
HCG is used to trigger ovulation
Treatment:
Drug: HCG trigger

Trial contacts and locations

1

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Central trial contact

Usama M Fouda, Prof.

Data sourced from clinicaltrials.gov

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