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Dual Trigger Versus Booster Dose of HCG

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Infertility

Treatments

Drug: Human Chorionic Gonadotropin
Procedure: IVF/ICSI

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

To salvage the luteal phase and improve pregnancy rate in antagonist IVF/ICSI cycles triggered with GnRH agonist. Two strategies are compared dual trigger with GnRH agonist plus 1000 IU of HCG or triggering with GnRH and giving a booster dose of HCG (1500 IU) on the day of ovum pickup.

Enrollment

200 patients

Sex

Female

Ages

20 to 37 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • High responder females undergoing antagonist protocol IVF/ICSI cycle
  • More than 14 MII oocytes
  • Estradiol more than 3500 pg/ml on day of trigger

Exclusion criteria

  • Any other protocol
  • Normal or poor responders

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

Dual trigger
Active Comparator group
Description:
GnRH agonist plus 1000 IU of HCG to trigger final maturation
Treatment:
Procedure: IVF/ICSI
Drug: Human Chorionic Gonadotropin
Booster HCG dose
Active Comparator group
Description:
GnRH agonist only to trigger final maturation followed by a booster dose of 1500 IU of HCG on the day of ovum pickup
Treatment:
Procedure: IVF/ICSI
Drug: Human Chorionic Gonadotropin

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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