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Completed

NCT Number: NCT03349190

Impact of Esmya on Fertility to Infertile Women With Fibroids Managed With Assisted Reproduction Techniques

Fibroid is a frequent pathology of infertile women. Its deleterious effect on the infertility would be due to the mechanical way.

The interest of the resection of intramural fibroids is discussed. It is necessary to measure the indication of a myomectomy, whatever the surgical procedure. On the one hand, it may cause important potential complications, and on the other hand, the surgery does not improve the parameters of the fertility.

Thus, it is a major stake to avoid the surgical operation. A decrease of the size of these fibroids by medical treatment is then a good option.

When the surgical treatment is necessary, a medical pre-surgical treatment is often proposed in order to decrease the symptomatology and to reduce the size of the fibroid to facilitate the surgery.

Acetate Ulipristal (UPA) has been marketed in this indication. Following the Pearl I-II studies, the first indication in France was a pre-surgical treatment for 3 months at a dose of 5 mg per day.

The Pearl III and IV studies evaluated the Esmya® administration as a long-term intermittent repeated treatment, giving to it a prominent position for the long-term management of symptomatic fibroids.

Furthermore, cases of pregnancy before surgery are frequently described in women with fibroids treated by UPA for a pre-IVF surgery.

5 to 10 % of women who are managed for infertility have fibroids and only 2% to 3% have this unique cause of infertility.

Then, some of patients followed in ART centers have been treated by UPA to reduce the fibroids size and/or to decrease the associate symptoms.

The aim of this study is to evaluate in the different French ART centers, the impact on fertilization of UPA administration for infertile women with fibroids and to describe the modalities of its prescriptions and to collect information regarding safety tolerance profile of Esmya® in this patient population.

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Key information

Age range

18 year–43 year

Sex eligibility

Female

Study type

Observational

Primary location

Chu Angers, Angers, France

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About this study

A retrospective, national, multicenter study

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age between 18 to 43 years 'old at the time of the beginning of ulipristal acetate intake
  • Women with fibroid at the time of ulipristal acetate prescription
  • Women with desire to have children and managed for infertility in an ART center (whatever the type of infertility treatment)
  • Women having received a treatment by ulipristal acetate
  • Data collected between 2013/12/01 and 2018/06/30 ; data collected between ulipristal acetate prescription until the term of pregnancy or embryo transfer failure (up to 4) or death/lost to follow up or ART treatment discontinuation

Exclusion criteria

none

Treatment and study plan

Ulipristal Acetate

Drug

Ulipristal Acetate (Esmya) administrated for fibroids indication before surgery and IVF/ICSI procedure(retrospective study)

Primary outcomes

  1. Clinical pregnancy

    Time frame: 15 days

    Clinical pregnancy rate after maximum 4 embryos transferred by IVF/ICSI procedures ; pregnancy is defined by beta-hCG> 1000 or presence of a gestation sac

Secondary outcomes

  1. Spontaneous pregnancy

    Time frame: at least 2 months

    Spontaneous pregnancy rate before first embryo transferred by IVF/ICSI procedures; pregnancy is defined by beta-hCG > 1000 or presence of a gestation sac

  2. Live birth / miscarriage

    Time frame: 9 months

    Live birth rate / miscarriage rate

  3. Fibroids size

    Time frame: Baseline (before ulipristal acetate administration) and 20 months

    Fibroids size reduction

  4. Surgery rate

    Time frame: 3 months

    Rate of surgery

  5. Surgery description

    Time frame: 3 months

    Description of the surgery type and surgery indication

  6. Description of ulipristal acetate prescription

    Time frame: 20 months

    Reasons of the prescription, type of fibroids concerned, number of cycles of treatment, treatment duration

  7. Safety impact on ulipristal acetate administration

    Time frame: 20 months

    Review of adverse drug reactions resulting in ulipristal acetate treatment modification or discontinuation

  8. Ulipristal acetate safety analysis in infertile women with fibroids

    Time frame: 20 months

    Review of all serious adverse reactions (expected or unexpected) in this population

Sponsors and collaborators

Lead sponsor

ASSOCIATION POUR LE DEVELOPPEMENT EN FECONDATION IN VITRO

Other

Collaborators

  • Gedeon Richter Plc.

Registry information

Official study title

A Retrospective, National, Multicenter Study Evaluating the Impact of Ulipristal Acetate (Esmya®) on Infertility to Infertile Women With Fibroids Managed With Assisted Reproduction Techniques (ART)

Acronym: NACRE

Important dates

Study start
2017
Primary completion
2018
Study completion
2019
First posted
Nov 21, 2017
Registry last updated
Jan 9, 2019

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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