Skip to main content
OpenTrials
Completed

NCT Number: NCT03161340

Immunomodulatory Effects of Rapamycin on Pregnancy Rate of Patient With Recurrent Implantation Failure

Repeated implantation failure (RIF) is determined as failure to achieve pregnancy following at least 3 embryo transfers of high quality embryos in IVF cycles. Successful implantation and pregnancy depend on the activity of a variety of factors such as adhesion molecules, cytokines and immune cells.The process by which the foreign conceptus is accepted requires the appropriate function of regulatory T cells (Treg), which are known as the mediators of immune regulation. Tregs are capable of inducing maternal tolerance toward the fetus and their systemic expansion has been observed in early pregnancy. Furthermore, Th17 cells that play important roles in mounting inflammation are involved in the maintenance of pregnancy as a subset of effector T cells.The mammalian target of rapamycin (mTOR) inhibitors are immunosuppressive agents used after solid organ transplantation. Sirolimus as the most common mTOR inhibitor is able to effectively prevent allograft rejection and possesses significant antitumor properties. Pregnancy is a state of immunosuppression and the dysregulated immune responses has been observed in women with RIF. Accordingly, modulation of the immune system by an immunosuppressant drug may present an approach to overcome implantation failure. In this context, the use of Sirolimus might offer promise to achieve a better pregnancy outcome among women with implantation failure who undergo IVF. Based on previous findings, we hypothesized that Sirolimus may be beneficial for the improvement of pregnancy rate in women with IVF failure.

In the current study, we performe randomized phase II clinical trial to determine whether Sirolimus could be used as a bona fide treatment to increase the success rate of IVF in women with RIF of immune etiologies.A total 121 patients with a history of at least 3 RIF after IVF/ET cycles that will refer to Eastern Azerbaijan ACECR ART center, Alzahra Hospital of Tabriz University of Medical Sciences and Infertility Treatment center ACER Qom from July 2017 to June 2018 were select and enroll in this multicenter, randomized, double-blind, phase II study.

Normal ranges for Th17/Treg cell ratios establish using 50 normal fertile women who had a history of normal delivery by natural conception.

In patients with elevated Th17/Treg ratios, half of them treat with Sirolimus (Rapamune®; Pfizer, UK) and rest of patients not treat (control group). The patients in the treatment group will began Sirolimus 2 days prior to embryo transfer (ET) and will continue until the day of pregnancy test (15 day after ET), for a total of 17 days Sirolimus administe in a daily dose of 2mg.

Completed

Looking for future studies?

Notify Me

Key information

Age range

20 year–41 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Qom ACECR ART Center, Qom, Iran

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • The patients selected for this study will be with elevated Th17/Treg ratio
  • Enrolled patients will experience at least 3 times we have consecutive defeats implantation.
  • Patients in the study will record their medical history do not have any type of immunotherapy.

Exclusion criteria

  • Our criteria for exclusion of patients from the study include the following:
  • Patients aged 20 years and above 41 years
  • Patients or their spouse has abnormal karyotype or chromosomal and genetically disorders.
  • Patients who have bleeding problems.
  • Patients who have chronic disorders those are forced to use the specific drug.
  • Patients who test HIV, hepatitis C virus (HCV) or hepatitis C virus (HBV) are positive.
  • Patients who have a history of asthma and allergies to certain drugs.
  • Patients who have abnormalities of the uterus

Treatment and study plan

Rapamycin

Drug

Patients will take Rapamycin 2 days before IVF until 15 days after IVF

Other names: Treatment group

Primary outcomes

  1. Changes in Treg cells

    Time frame: 2 days before IVF until 15 days after IVF

    Flowcytometry

  2. Changes in mRNA expression of cytokines related to Treg cells

    Time frame: 2 days before IVF until 15 days after IVF

    quantitative polymerase chain reaction (qPCR)

  3. Changes in mRNA expression of cytokines related to Th17 cells

    Time frame: 2 days before IVF until 15 days after IVF

    quantitative polymerase chain reaction (qPCR)

  4. Changes in secretion levels of cytokines related to Treg cells

    Time frame: 2 days before IVF until 15 days after IVF

    Elisa

  5. Changes in secretion levels of cytokines related to Th17 cells

    Time frame: 2 days before IVF until 15 days after IVF

    Elisa

  6. Changes in mRNA expression levels of transcription factors related to Th17 cells

    Time frame: 2 days before IVF until 15 days after IVF

    quantitative polymerase chain reaction (qPCR)

  7. Changes in mRNA expression levels of transcription factors related to Treg cells

    Time frame: 2 days before IVF until 15 days after IVF

    quantitative polymerase chain reaction (qPCR)

  8. Changes in expression levels of miRNAs

    Time frame: 2 days before IVF until 15 days after IVF

    quantitative polymerase chain reaction (qPCR)

Secondary outcomes

  1. Pragnancy rate

    Time frame: 2 days before IVF until 15 days after IVF

    Beta-human Chorionic Gonadotrophin (ΒHCG) protein assay

  2. Pregnancy Rate

    Time frame: 2 days before IVF until 15 days after IVF

    Ultrasonography

  3. Live birth

    Time frame: After about 9 months of positive βhCG test

    The birth of a living child

Sponsors and collaborators

Lead sponsor

Mehdi Yousefi

Other

Registry information

Official study title

Effect of Rapamycin on Pregnancy Rate of Patient With Recurrent Implantation Failure With Immunological Causes

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
May 19, 2017
Registry last updated
Apr 10, 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.

Published trials that share one or more normalized conditions with this study.