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hCG Supplementation in Frozen-Thawed Embryo Transfer Cycle

H

Hadassah Medical Center

Status and phase

Completed
Phase 2

Conditions

Fertility Agents, Female

Treatments

Drug: s.c. human chorionic gonadotropin (Ovitrelle)

Study type

Interventional

Funder types

Other

Identifiers

NCT00398229
freezehcg-HMO-CTIL

Details and patient eligibility

About

The implantation rate after frozen-thawed embryo transfer cycles depends mostly on the receptivity of the endometrium and the embryo quality.The effects of human chorionic gonadotropins (hCG) on the endometrium have been investigated for several years. hCG was shown to up-regulate gene expression during the differentiation of human endometrial stromal cells into decidua. The aim of our study was to assess the benefit of hCG supplementation throughout the secretory phase of artificial frozen-thawed embryo transfer cycles.

Enrollment

300 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • all women on frozen-thawed embryo-transfer cycle

Exclusion criteria

  • any allergy to injection of human chorionic gonadotropin before

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 2 patient groups, including a placebo group

A
Active Comparator group
Description:
receiving hCG injection
Treatment:
Drug: s.c. human chorionic gonadotropin (Ovitrelle)
B
Placebo Comparator group
Treatment:
Drug: s.c. human chorionic gonadotropin (Ovitrelle)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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