Dienogest Versus GnRH-a Pre-treatment in Women With Endometriosis Undergoing IVF

American University of Beirut Medical Center

Status: Unknown

Conditions: Endometriosis

Treatments: Drug: gonapeptyl; Procedure: IVF/IVF+ART; Drug: Dienogest 2 MG

Study type: Interventional

Funder types: Other

Identifiers

NCT03142035

OGY.DC.03

Details and patient eligibility

About

Endometriosis is a chronic gynecologic disease that affects approximately 10% of women in the reproductive age group . It is characterized by the presence of endometrial tissue outside the uterus, causing pelvic pain and subfertility. It is estimated that around 40% of infertile women have the diagnosis of endometriosis . Infertility secondary to endometriosis is thought to be multifactorial. Women with endometriosis often require in vitro fertilization (IVF). One medical intervention that has been shown to improve IVF outcomes in women with endometriosis is hormonal suppression with gonadotropic releasing hormone agonist (GnRH-a) for a period of 3 to 6 months .

In recent years, the effectiveness of dienogest, a fourth-generation progestin, for endometriosis treatment has been demonstrated. Dienogest seems to be as effective as GnRH-a in improving endometriosis-related pelvic pain [4]. However, no study has yet assessed whether dienogest has any benefit in treating endometriosis associated infertility.

The aim of our study is to evaluate the efficacy of dienogest versus GnRH-a in improving ongoing pregnancy rates in women undergoing IVF due to endometriosis. We will conduct a non-blinded randomized controlled trial. One group will receive dienogest 2mg daily for a period of 3 months followed by a standard IVF/Intracytoplasmic Sperm Injection (ICSI) cycle. The second group will receive one injection of 3.75mg of GnRH-a every 28 days for three doses followed by a standard IVF/ICSI cycle 3 months later. The third group will not receive any medical interventions before the planned IVF/ICSI cycle. We hypothesize that patients receiving dienogest will have similar ongoing pregnancy rates compared to patients receiving the GnRH-a injection. Secondary outcomes including number of gonadotropins consumed, number of stimulation days, number of metaphase II eggs retrieved, fertilization rate, embryo quality, miscarriage rate, clinical pregnancy rates, live birth rates and potential maternal and obstetrical complications will also be evaluated. We will also compare ongoing pregnancy rates between the groups receiving Dienogest and placebo, and GnRH agonist and placebo.

Enrollment: 189 estimated patients

Sex: Female

Ages: 18 to 38 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Primary or secondary infertility
• Endometriosis, stage III - IV, confirmed surgically by laparoscopy or laparotomy and/or radiologically by the presence of endometrioma on pelvic ultrasound or magnetic resonance imaging (MRI)
• Normal uterine cavity assessed by hysteroscopy or hysterosalpingogram
• Normal hormonal profile: TSH, prolactin, fasting blood sugar
• Normal semen analysis and mild/moderate male factor (Total motile sperm count > 5 million/ml and/or normal WHO morphology >20%)
• First IVF cycle or history of failed IVF cycles
• Washout period of ≥6 months after any diagnostic or therapeutic surgery for endometriosis or after any medical treatment with Dienogest or GnRH agonist.

Exclusion criteria

• • Low ovarian reserve defined by one of the following: low AMH ≤1.5ng/mL and/or basal day 3 FSH ≥ 10mIU/mL and/or basal day 3 Estradiol ≥ 60ng/mL and/or previous egg collection yield of ≤3 oocytes.

  • Absolute contraindications to dienogest, including:

• undiagnosed abnormal vaginal bleeding

• pregnancy and/or lactation

• active venous thromboembolic disorder

• history of or current arterial and cardiovascular disease (eg, MI, CVA)

• diabetes mellitus with vascular involvement

• history of or current severe hepatic disease where liver function tests remain abnormal

• history of or current hepatic neoplasia (benign or malignant)

• known or suspected sex-hormone-dependent malignancy

• ocular lesions due to ophthalmic vascular disease, such as partial or complete vision loss or defect in visual fields

• current or history of migraine with focal aura

• hypersensitivity or poor tolerance to dienogest

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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189 participants in 3 patient groups

Dienogest

Experimental group

Description:

patients will receive daily dienogest (2mg) for a total of 3 months (84 days)

Treatment:

Drug: Dienogest 2 MG

Procedure: IVF/IVF+ART

GnRH agonist

Active Comparator group

Description:

patients will receive a single GnRH-a injection (3.25mg) every 28 days for three months.

Treatment:

Procedure: IVF/IVF+ART

Drug: gonapeptyl

Control Group

Other group

Description:

patients will not receive any medical intervention and will proceed with their IFV/ICSI cycles.

Treatment:

Procedure: IVF/IVF+ART