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The Effect of Luteinizing Hormone (LH) Supplementation Following Gonadotropin-releasing Hormone (GnRH) Antagonist Administration in Advanced Reproductive Ageing Women Undergoing IVF and Embryo Transfer (IVF/ET)

B

Baruch Padeh Medical Center

Status and phase

Completed
Phase 4

Conditions

Pregnancy Result Rape

Treatments

Drug: Leuveris

Study type

Interventional

Funder types

Other

Identifiers

NCT01016210
Leuveris1.CTIL

Details and patient eligibility

About

To explore whether recombinant LH (rLH) supplementation (Leuveris) to recombinant follicle stimulating hormone (rFSH) following GnRH antagonist treatment has an advantage in infertile women with advanced reproductive ageing undergoing IVF-ET.

Enrollment

60 estimated patients

Sex

Female

Ages

25 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • female candidate to IVF
  • between 30-45 years old

Exclusion criteria

  • not included for fertilization

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

60 infertile women
Experimental group
Description:
Candidates for IVF-ET treatment
Treatment:
Drug: Leuveris
Drug: Leuveris
control
No Intervention group
Description:
no treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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