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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03161340
Other study ID # TabrizUMS-infertility-001
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date July 11, 2017
Est. completion date June 20, 2018

Study information

Verified date April 2019
Source Tabriz University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 121
Est. completion date June 20, 2018
Est. primary completion date May 9, 2018
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 41 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Iran, Islamic Republic of Qom ACECR ART Center Qom
Iran, Islamic Republic of Estern Azarbaijan ACECR ART center Tabriz

Sponsors (1)

Lead Sponsor Collaborator
Mehdi Yousefi

Country where clinical trial is conducted

Iran, Islamic Republic of, 

References & Publications (8)

Calleja-Agius J, Muttukrishna S, Pizzey AR, Jauniaux E. Pro- and antiinflammatory cytokines in threatened miscarriages. Am J Obstet Gynecol. 2011 Jul;205(1):83.e8-16. doi: 10.1016/j.ajog.2011.02.051. Epub 2011 Feb 23. — View Citation

Nakagawa K, Kwak-Kim J, Ota K, Kuroda K, Hisano M, Sugiyama R, Yamaguchi K. Immunosuppression with tacrolimus improved reproductive outcome of women with repeated implantation failure and elevated peripheral blood TH1/TH2 cell ratios. Am J Reprod Immunol. — View Citation

Ozkan ZS, Deveci D, Simsek M, Ilhan F, Risvanli A, Sapmaz E. What is the impact of SOCS3, IL-35 and IL17 in immune pathogenesis of recurrent pregnancy loss? J Matern Fetal Neonatal Med. 2015 Feb;28(3):324-8. doi: 10.3109/14767058.2014.916676. Epub 2014 Ma — View Citation

Santos MA, Kuijk EW, Macklon NS. The impact of ovarian stimulation for IVF on the developing embryo. Reproduction. 2010 Jan;139(1):23-34. doi: 10.1530/REP-09-0187. Review. — View Citation

Sugiura-Ogasawara M, Suzuki S, Ozaki Y, Katano K, Suzumori N, Kitaori T. Frequency of recurrent spontaneous abortion and its influence on further marital relationship and illness: the Okazaki Cohort Study in Japan. J Obstet Gynaecol Res. 2013 Jan;39(1):12 — View Citation

Wang L, Harris TE, Roth RA, Lawrence JC Jr. PRAS40 regulates mTORC1 kinase activity by functioning as a direct inhibitor of substrate binding. J Biol Chem. 2007 Jul 6;282(27):20036-44. Epub 2007 May 17. — View Citation

Winger EE, Reed JL, Ji X. First-trimester maternal cell microRNA is a superior pregnancy marker to immunological testing for predicting adverse pregnancy outcome. J Reprod Immunol. 2015 Aug;110:22-35. doi: 10.1016/j.jri.2015.03.005. Epub 2015 Apr 16. — View Citation

Winger EE, Reed JL. Low circulating CD4(+) CD25(+) Foxp3(+) T regulatory cell levels predict miscarriage risk in newly pregnant women with a history of failure. Am J Reprod Immunol. 2011 Oct;66(4):320-8. doi: 10.1111/j.1600-0897.2011.00992.x. Epub 2011 Fe — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in Treg cells Flowcytometry 2 days before IVF until 15 days after IVF
Primary Changes in mRNA expression of cytokines related to Treg cells quantitative polymerase chain reaction (qPCR) 2 days before IVF until 15 days after IVF
Primary Changes in mRNA expression of cytokines related to Th17 cells quantitative polymerase chain reaction (qPCR) 2 days before IVF until 15 days after IVF
Primary Changes in secretion levels of cytokines related to Treg cells Elisa 2 days before IVF until 15 days after IVF
Primary Changes in secretion levels of cytokines related to Th17 cells Elisa 2 days before IVF until 15 days after IVF
Primary Changes in mRNA expression levels of transcription factors related to Th17 cells quantitative polymerase chain reaction (qPCR) 2 days before IVF until 15 days after IVF
Primary Changes in mRNA expression levels of transcription factors related to Treg cells quantitative polymerase chain reaction (qPCR) 2 days before IVF until 15 days after IVF
Primary Changes in expression levels of miRNAs quantitative polymerase chain reaction (qPCR) 2 days before IVF until 15 days after IVF
Secondary Pragnancy rate Beta-human Chorionic Gonadotrophin (?HCG) protein assay 2 days before IVF until 15 days after IVF
Secondary Pregnancy Rate Ultrasonography 2 days before IVF until 15 days after IVF
Secondary Live birth The birth of a living child After about 9 months of positive ßhCG test
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