Current partner codePEPTIDESDE
NCT02912988·Phase 3·INTERVENTIONAL

Letrozole in Stimulated IVF Cycles

Status

Completed

Phase

Phase 3

Enrollment

900

Locations

2

Results

Not posted

Publications

1

Study summary

What the protocol is testing.

In-vitro fertilization (IVF) is the treatment of choice for couples with prolonged infertility. The treatment usually involves hormonal stimulation of the ovaries by follicle stimulating hormone (FSH), followed by surgical removal of eggs which are then mixed with sperm in the laboratory to create embryos. The success rates of IVF treatment remain unsatisfactory and are no longer increasing. One of the reasons is an adverse effect of high serum estradiol levels following FSH stimulation on the lining of the uterus. Letrozole is a drug used in the prevention of recurrence of breast cancer because of its action to reduce the intra-ovarian aromatization of androgens to estrogens. It is now increasingly used for ovulation induction and is as safe as clomiphene citrate. Use of letrozole during standard ovarian stimulation for IVF producing adequate numbers of oocytes with physiological levels of estradiol may increase the present success rate of standard IVF treatment. The aim of this randomized study is to compare the live birth rate of FSH alone versus combined FSH and letrozole used for ovarian stimulation in IVF treatment.

Full detailed description

Trial design: Infertile women undergoing IVF treatment will be randomized into one of the following two groups by an online randomization program: Letrozole group: letrozole 2.5mg daily will be given at the start of the antagonist during ovarian stimulation i.e. day 5 of stimulation. Control group: standard care with FSH alone during ovarian stimulation. Intervention: Subjects can be put on oral contraceptive pill in the preceding cycle for scheduling stimulation. On day 2-3, a pelvic ultrasound will be performed for antral follicle count. Letrozole group: Daily 150-225 IU human menopausal gonadotrophin (HMG) / Follicle stimulating hormone (FSH) from cycle day 2-4 (at least 5 days after stopping the oral contraceptive pill) and co-treatment with letrozole 2.5 mg daily from stimulation day 5 until the day before hCG administration. GnRH antagonist (cetrotide or orgalutran) 0.25 mg daily from stimulation day 5 until the day of hCG administration. Control group: Daily 150-225 IU HMG/FSH cycle day 2-4 (at least 5 days after stopping the oral contraceptive pill) until the day before hCG administration. GnRH antagonist 0.25 mg daily from stimulation day 5 until the day of hCG administration. A blood sample will be taken and analyzed in the local laboratory for serum E2, P and testosterone levels on cycle day 2 or 3 (baseline) and day of hCG (or the day before). The remaining serum will be frozen and stored for later analysis. A sample of follicular fluid (FF) will be collected from the first blood free follicle. The FF will be frozen and stored for later analysis: Estradiol, testosterone, inhibin B and AMH levels. All techniques of IVF including harvesting of oocytes, insemination with specially prepared sperm, embryo culture in the laboratory, embryo transfer and luteal phase support will be according to local protocols. One or two embryos or blastocysts will be replaced. A pregnancy test will be carried out 2 weeks after embryo transfer in both arms. All women who have a positive pregnancy test 2 weeks after embryo transfer will undergo a transvaginal ultrasound scan to identify the presence and number of gestation sac with a fetal heart signifying an ongoing pregnancy. Pelvic scan will be repeated at 8 weeks, 12 weeks, 24 weeks and 36 weeks of gestation for fetal growth.

Interventions

Treatment arms and agents.

DRUG

Letrozole

Daily 150-300 IU human menopausal gonadotrophin (HMG) / Follicle stimulating hormone (FSH) from cycle day 2-4 (at least 5 days after stopping the oral contraceptive pill) and co-treatment with letrozole 2.5 mg daily from stimulation day 5 until the day before hCG administration. GnRH antagonist (cetrotide or orgalutran) 0.25 mg daily from stimulation day 5 until the day of hCG administration.

Timeline

From registration to results.

  1. First posted

    Sep 23, 2016

  2. Study start

    Mar 1, 2018

  3. Primary completion

    Apr 30, 2022

  4. Study completion

    Apr 30, 2023

  5. Results posted

    Not reported

  6. Registry updated

    May 10, 2023

Outcomes

What the study measures.

Primary outcomes

Live birth rate

Time frame · through study completion, an average of 1 year

A baby born alive after 20 weeks gestation

Secondary outcomes

Miscarriage rate

Time frame · up to 20 weeks of gestation

Miscarriage before 20 weeks gestation

Clinical and ongoing pregnancy rates

Time frame · up to 20 weeks

Presence of at least one gestational sac on ultrasound at 6 weeks and 8-10 weeks

Ovarian hyperstimulation rate

Time frame · about 1 month

Ovarian hyperstimulation rate classified according to Royal College of Obstetrics and Gynaecology of the United Kingdom

Total IU of FSH used per cycle

Time frame · about 2 weeks

Total IU of FSH used per cycle

Number of follicles > 12 mm on day of hCG (or the day before)

Time frame · about 2 weeks

Transvaginal ultrasound performed to measure and the follicles on day of hcG or the day before.

Number of oocytes obtained

Time frame · On the operation day of transvaginal ultrasound guided oocyte retrieval

Number of oocyte obtained during the operation of transvaginal ultrasound guided oocyte retrieval

Proportion of oocytes resulting in top quality day 2 (or day 3) embryos according to validated morphological criteria.

Time frame · 2-3 days after the transvaginal ultrasound guided oocyte retrieval operation

Proportion of oocytes resulting in top quality day 2 (or day 3) embryos according to validated morphological criteria.

Oocyte fertilization rate

Time frame · 2-3 days after the transvaginal ultrasound guided oocyte retrieval operation

Oocyte fertilization rate

Number and quality of embryos obtained

Time frame · 2-3 days after the transvaginal ultrasound guided oocyte retrieval operation

Number and quality of embryos obtained

Endometrial thickness on day of hCG (or the day before)

Time frame · on day of hCG (or the day before)

Endometrial thickness on day of hCG (or the day before) measured by transvaginal ultrasound

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
42 Years
Sex
FEMALE
Healthy volunteers
No

Inclusion Criteria: * women under 42 years of age * medical indication for IVF treatment * antral follicle count prior to ovarian stimulation \>=3 * informed consent Exclusion Criteria: * women using donor oocytes * women undergoing preimplantation genetic diagnosis * women with abnormal uterine cavity shown on hysterosalpingogram or saline infusion sonogram * women with hydrosalpinges shown on scanning and not corrected * previous documented poor response (\<=3 oocytes) to ovarian stimulation using at least FSH 225 IU daily

Study locations

2 registered sites.

China. Showing up to 24 locations stored in the fast local snapshot.

Department of Obstetrics and Gynaecology

Hong Kong, Hong Kong, China

Peking University Third Hospital

Beijing, China

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Put the record in context.

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