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Ulipristal Acetate on Progesterone Levels and Glycodelin-A Endometrial Pattern

Effect of Ulipristal Acetate Administration on Serum Progesterone Levels and Glycodelin-A Endometrial Pattern in Women Undergoing Controlled Ovulation Stimulation.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01391845
Enrollment
16
Registered
2011-07-12
Start date
2011-07-31
Completion date
2012-06-30
Last updated
2011-07-20

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

Conditions

Infertility

Keywords

progesterone, glycodelin-A, ulipristal acetate

Brief summary

Controlled ovarian stimulation (COS) for FIV increases progesterone (P) and estradiol (E2) serum levels in supraphysiologic concentrations at the end of follicular phase. Elevated serum P levels leads to an accelerated endometrial maturation which interferes with the dialogue between embryo and endometrium. It has been reported that serum progesterone levels ≥ 1.5 ng/ml on the last day of COS are related to a significant decrease in the ongoing pregnancy rate following IVF cycles. Also, it has been reported a significant alteration in the endometrial gene expression profile related to P elevated levels. Glycodelin-A is an immunomodulatory glycoprotein synthesized by luteal-phase endometrial epithelium and its expression seems to be related to the action of P. Because glycodelin-A has immunosuppressive activity, it may facilitate the process of implantation and the maintenance of pregnancy. It is already know that ulipristal acetate (UPA) decrease serum P levels. The hypothesis of this study is that UPA is been able to modify P serum levels and glycodelin-A endometrial expression pattern on FSH/GnRH Antagonist cycles for FIV.

Detailed description

Controlled ovarian stimulation (COS) for FIV increases progesterone (P) and estradiol (E2) serum levels in supraphysiologic concentrations at the end of follicular phase. Elevated serum P levels leads to an accelerated endometrial maturation which interferes with the dialogue between embryo and endometrium. It has been reported that serum progesterone levels ≥ 1.5 ng/ml on the last day of COS are related to a significant decrease in the ongoing pregnancy rate following IVF cycles. Also, it has been reported a significant alteration in the endometrial gene expression profile related to P elevated levels. Glycodelin-A is an immunomodulatory glycoprotein synthesized by luteal-phase endometrial epithelium and its expression seems to be related to the action of P. Because glycodelin-A has immunosuppressive activity, it may facilitate the process of implantation and the maintenance of pregnancy. Objective: to evaluate the endometrial effect of Progesterone through Glycodelin-A expression pattern on women exposed or not to ulipristal acetate in GnRH Antagonist cycles using two different doses of FSH for ovarian controlled stimulation. Methods: prospective controlled randomized study. It will be enrolling 16 oocytes donors from Oocyte Donation Program of PROAR (a Reproductive Center of Rosario, Argentina). On day 3 of menstrual cycle FSH serum levels and antral follicular count (AFC) will be measure. If those results fulfill with inclusions criteria, patients will be randomize for FSH 225UI or 300UI GnRH-Antagonist/ urinary FSH protocol. P serum levels will be measure every 48 hours since at least 1 follicle ≥14 mm will be achieve until at least 1 follicle reach 19mm of diameter. The next day of hCG administration a new P circulating will be measure and then the patient will be randomize trough opaque envelopes for receive 30mg of ulipristal acetate or placebo. An endometrial biopsy with Cornier´s Pipelle will be performing 3 and 5 days after hCG injection (hCG+3 and hCG+5 days) to evaluate endometrial dating and Glycodelin-A expression pattern. Statistical analysis: nominal variables will be analyzing using t-Student test and the effect of ulipristal with ANOVA.

Interventions

DRUGulipristal acetate

30mg of ulipristal acetate orally the day of hCG injection in a unique dose

DRUGplacebo

placebo orally in a unique dose the day of hCG injection

Sponsors

Programa de Asistencia Reproductiva de Rosario
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Age \<35 years old * FSH on day 3: \<12 UI/ml * Antral follicular count ≥ 6 on day 3 of the cycle * BMI: \<30 Kg/m2

Exclusion criteria

* Hypothyroidism * Hyperprolactinemia * Kidney or liver disease * Smoking * Alcoholism

Design outcomes

Primary

MeasureTime frameDescription
Changes in Glycodelin-A endometrial expression pattern and Progesterone serum levels in women expose to ulipristal acetate on stimulated ovarian cycles for FIVparticipants will be followed for the duration of one mesntrual cycle, from day 1 of the cycle until day 28-32to evaluate Glycodelin-A expression pattern by immunohistochemistry and Progesterone serum levels on women exposed or not to ulipristal acetate in FSH/GnRH Antagonist protocol.

Secondary

MeasureTime frame
P levels during controlled ovarian stimulation since at least one follicle achieve ≥14mm of diameterparticipants will be followed for the duration of one mesntrual cycle,from day 1 until day 28-32
Serum P levels on two different doses of FSH in a GnRH Antagonist protocol for ovarian stimulationparticipants will be followed for the duration of one mesntrual cycle,from day 1 until day 28-32
Glycodelin-A endometrial expression pattern on two different doses of FSH in a GnRH Antagonist protocol for ovarian stimulationparticipants will be followed for the duration of one mesntrual cycle, from day 1 until day 28-32

Countries

Argentina

Contacts

Primary ContactIdelma Serpa, MD
idelmaserpa@yahoo.com.ar+54 0341 155668963
Backup ContactIdelma Serpa, MD
idelmaserpa@yahoo.com.ar

Outcome results

None listed

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