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Evaluation of the Luteolytic Effect of a Gonadotropin Releasing Hormone (GnRH) Agonist After the Administration of Human Chorionic Gonadotropin (hCG) in the Initial Follicular Phase a Its Influence on the Prognosis of in Vitro Fertilization Treatment

Evaluation of the Luteolytic Effect of a Gonadotropin Releasing Hormone (GnRH) Agonist After the Administration of Human Chorionic Gonadotropin (hCG) in the Initial Follicular Phase a Its Influence on the Prognosis of in Vitro Fertilization Treatment

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00948805
Enrollment
25
Registered
2009-07-29
Start date
2009-01-31
Completion date
2010-07-31
Last updated
2009-07-29

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

Conditions

Infertility

Keywords

corpus luteum rescue, Gonadotropin Releasing Hormone (GnRH agonist), human Chorionic Gonadotropin (hCG), infertility, pregnancy rate

Brief summary

This study was designed to evaluate the ability of gonadotropin releasing hormone (GnRh) agonist to prevent the rise of progesterone during controlled ovarian stimulation for in vitro fertilization (IVF) after the administration of human Chorionic Gonadotropin (hCG) on the first day of menses.

Detailed description

The aim of this study is to evaluate the efficacy of a GnRH agonist in preventing the functional rescue of corpus luteum in women submitted to controlled ovarian stimulation with administration of hCG on the first day of menses and to evaluate its effect on pregnancy rate and ovarian steroidogenesis.

Interventions

DRUGGnRH agonist

3,6mg of goserelin acetate, 250mg of hCG, FSH variable dose according to the number of days required for appropriate ovarian stimulation

DRUGControl

250mg of hCG, Zoladex, FSH variable dose according to the number of days required for appropriate ovarian stimulation

Sponsors

University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 38 Years
Healthy volunteers
Yes

Inclusion criteria

* age \>21 and \< 38 years old * polycystic ovarian syndrome * risk for ovarian hyperstimulation syndrome

Exclusion criteria

* recurrent abortion * endometriosis * more than 3 IVF failures * use of oral contraceptive pills in the preceding 3 months * low response to gonadotropins

Design outcomes

Primary

MeasureTime frame
Frequency of functional rescue of corpus luteum6 months

Secondary

MeasureTime frame
Pregnancy rate6 months
Levels of serum steroids6 months
Levels of serum gonadotropins6 months

Countries

Brazil

Contacts

Primary ContactCláudia M Gomes, MD
cgomes@huntington.com.br551130596122
Backup ContactAndré M Rocha, PhD
arocha@huntington.com.br551130596122

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026