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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03081325
Other study ID # BL2015007
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received March 8, 2017
Last updated April 9, 2018
Start date March 2015
Est. completion date July 20, 2017

Study information

Verified date April 2018
Source Nanjing University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Recurrent miscarriage(RM) and recurrent implantation failure (RIF) are clinical challenge for clinicians and patients who are desperate for a healthy child.The specific etiology contains chromosomal abnormalities, reproductive anatomical abnormalities, endocrine disorders, reproductive system infections, autoimmune and environmental factors. However there are still 50% to 60% RM and RIF which don't have a clear cause,mainly associated with alloimmune factors.Among various treatments,lymphocytes active immunotherapy is the most common treatment method, and its clinical efficacy is widely recognized although its action mechanism is not clear so far.


Description:

The main mechanism of active immunotherapy includes upregulating Th2-type cytokines, downregulating Th1-type cytokines, making Th1 / Th2 shift to Th2, inducing maternal serum IL-6 and sIL6R, PIBF, EGF; inducing the expression of Fas / Fasl on lymphocyte surface; increasing the proportion of CD8 + cells, Th2-type cells and CD + CD25 + Treg cells, decreasing the activity of CD56 + CD16 + NK cell and so on.The purpose of this study is to observe the treatment effects of active immunotherapy on uRM and RIF patients. What's more,we will used flow cytometry, and quantitative real-time PCR (qPCR) methods to characterize Th1、Th2 and Treg cell populations after immunotherapy,ecpecting to find out the exact molecule mechanism of immunotherapy with paternal or third party lymphocytes.


Recruitment information / eligibility

Status Completed
Enrollment 292
Est. completion date July 20, 2017
Est. primary completion date June 2017
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- Healthy except for their history of recurrent abortions and were negative for blocking antibodies

- Willing to receive follow up

Exclusion Criteria:

- Patients with genetic impairment

- Patients with Mullerian anomaly

- Patients with hormonal deficiency

- Patients with metabolic disorder

- Patients with infectious disease

- Patients with autoimmune abnormalities

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
low-dose lymphocyte immunotherapy
Peripheral venous blood (PBMCs) was drawn from the husbands of uRM and RIF patients and then the PBMCs were resuspended and administered intradermally to uRM and RIF patients 3 times at 3-week intervals. Once conceived, the uRM and RIF patients undergo 2 rounds of treatment at 8-week intervals.

Locations

Country Name City State
China Reproductive Medicine Center, The Affiliated Drum Tower Hospital of Nanjing University Medical School Nanjing Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Nanjing University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary T cell proportion We use flow cytometry to detecte peripheral blood Th1?Th2 and Treg cells of uRM and RIF patients before and after low-dose lymphocyte immunotherapy to see if the immunotherapy have treatment effect on Th1/Th2/Treg paradigm disorder 1 year
Primary Abortion rate We undergo follow-up of all the uRM patients to see the abortion rate (miscarriage was confirmed by ultrasound before the 20th week of gestation) after lymphocyte immunotherapy 1 year
Primary IVF outcomes We observed the the implantation rate, clinical pregnancy rate, and ongoing pregnancy rate of RIF patients after low-dose lymphocyte immunotherapy 1 year