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Completed

NCT Number: NCT05166668

Letrozole /GnRH Antagonist Protocol in Women Over 40 Years Undergoing ICSI Cycle

The aim of this study To compare the clinical and laboratory outcomes of two ovarian stimulation protocols (standard GnRH antagonist protocol and aromatase inhibitor/ antagonist protocol) in women (40-44) years undergoing ICSI cycle.

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Key information

Conditions

Age range

40 year–44 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Menoufia University hospital

Shibīn al Kawm, Menoufia, 11111, Egypt

About this study

Fertility is known to decline significantly in women after the age of 35 years, and fecundity is almost completely lost after the age of 45 . As age increases the natural fecundity and pregnancy rates after assisted reproduction decrease .This reduction in fecundity is thought to be due to ovarian aging mainly, which is defined as a decline in both the quantity and quality of the ovarian follicle pool .The increase in patient's age is associated with poor ovarian response, as represented by smaller ovarian volume, lower antral follicle count and poor stromal vascularity. In addition to the reduction in fecundity, there is an increase in spontaneous abortion rates in this group of women .It has been reported that about 19% of all women undergo ART are 40 years, and they could be considered as expected poor responders .Various protocols of ovarian stimulation have been proposed to optimize IVF results in this age group, however, satisfactory results remain a challenge . The lack of initial central down-regulation in early follicular phase and adequate prevention of premature luteinizing hormone (LH) surge in late follicular phase provide GnRH antagonist protocol as a potentially proper option .The use of aromatase inhibitors in a GnRH antagonist protocol was suggested by some studies [Mit. Yarali and colleagues demonstrated that adjuvant therapy with letrozole could improve the response [Yarali et al., 2009]. Meanwhile, in another study, adding letrozole to ovarian stimulation has no positive effect on the likelihood of pregnancy . Letrozole is a selective, non-steroidal third generation aromatase inhibitor. Letrozole causes a reduction in conversion of androstenedione and testosterone to estrone and estradiol by inhibiting the aromatase enzyme activity . According to some published studies, the decline in early follicular phase estrogen levels, and consequently decrease in negative feedback of estrogen on FSH release in hypothalamic-pituitary axis cause an increase in endogenous gonadotropin secretion and stimulation of ovarian follicular growth. In addition, an increase in intraovarian androgens secondary to aromatase inhibition, augments the follicular sensitivity to FSH stimulation and follicular growth . Letrozole has no antiestrogenic effect over the endometrium . These reports prompted us to hypothesize that use of letrozole as a co-treatment agent in GnRH antagonist protocol might enhance cycle outcomes.

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women between 40- 44-years undergoing ICSI cycle with FSH less than 15 and AMH more than 0.30.

Exclusion criteria

  • Azoospermia in male partner,
  • Previous ovarian surgery,
  • Severe endometriosis,
  • Uterine cavity lesion
  • Metabolic or endocrine disorders including hyperprolactinemia and ypo/hyperthyroidism.
  • Previous failed ICSI cycle.
  • BMI more than 30.

Treatment and study plan

Letrozole 2.5Mg Tablet

Drug

letrozole (femara, Novartis) orally in a dose of 2.5 mg daily, on day 2 of cycle for 5 days and gonadotropins (300-450 IU) IM start on cycle day 3. then the dose modulated according to response

Other names: Gonadotropins units

Primary outcomes

  1. live birth rate

    Time frame: 1 year after embryo transfer

    deliveries ≥22 weeks gestation with heartbeat and breath

Secondary outcomes

  1. positive hCG

    Time frame: 2 weeks after FET

    serum β-hCG ≥10 mIU/mL

  2. clinical pregnancy

    Time frame: 5 weeks' gestation

    presence of intrauterine gestational sac by trans-vaginal ultrasound at gestational weeks.

  3. Total gonadotropin /cycle (IU),

    Time frame: two weeks

    number of gonadotropin units needed per cycle

  4. Duration of stimulation (Day),

    Time frame: two weeks

    number of days needed for stimulation

  5. Endometrial thickness (mm)

    Time frame: two weeks

    measure endometrial thickness

  6. serum E2 levels

    Time frame: two weeks

    measuring E2 level during stimulation

  7. Follicles number

    Time frame: two weeks

    number of follicles during stimulation

Sponsors and collaborators

Lead sponsor

Menoufia University

Other

Registry information

Official study title

Impact of Adding Letrozole to Gonadotrophin-Releasing Hormone Antagonist Protocol in Women Over 40 Years Undergoing ICSI Cycle

Important dates

Study start
2021
Primary completion
2025
Study completion
2025
First posted
Dec 22, 2021
Registry last updated
Feb 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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