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临床试验/NCT02946177
NCT02946177Unknown4 期

A Randomized Controlled Trial of the Effect of Influenza Vaccination on Implantation and Pregnancy Rates After Donor Egg Recipient In-Vitro Fertilization

Center for Human Reproduction1 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2017年1月19日最近更新:
适应症

试验速览

阶段
4 期
入组人数
126
试验地点
1
主要终点
Clinical Pregnancy

研究概览

简要总结

In this study the investigators propose a randomized controlled trial to evaluate the effect of influenza vaccination on clinical pregnancy rates among women undergoing in vitro fertilization as donor egg recipients.

详细描述

Since 2004 flu vaccination has been recommended by American College of Obstetricians and Gynecologists (ACOG) Advisory Committee on Immunization Practices (ACIP) for all pregnant women during flu season, regardless of the trimester of pregnancy. Many studies have examined the safety of influenza vaccination and found benefits beyond the simple prevention of maternal infection including the reduction of still birth. Recently evidence has emerged that women who have received a flu vaccination were less likely to experience premature labor. The investigators hypothesize that some of the maternal benefits of influenza vaccination might be based on other than prevention of the flu, possibly secondary to the induction of immune system pathways that favor immunological tolerance. Induction of immune system pathways that favor immunological tolerance has long been considered a possible path to improved embryo implantation and reduce miscarriages, though the topic is still somewhat controversial.

Patients undergoing donor egg recipient cycles will be randomized in two strata:

  1. History of recurrent miscarriage or implantation failure
  2. No history of recurrent miscarriage of implantation failure

Consenting patients will be randomized to receive either influenza vaccine or a saline placebo. Vaccination will occur 10 days before initiating anticipated menses or fertility treatment cycle start.

All patients will be receiving an offered a second injection at the time of negative pregnancy test or at the time of sign-out with a clinical pregnancy. The second injection will either be placebo or influenza vaccination depending on the original randomization. Patients and clinical staff will remain blinded to the original treatment assignment, except for the study coordinator and the single staff member assigned to administer the injection.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
21 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • All women preparing to undergo an oocyte donor recipient cycle
  • Women will only be allowed to participate in one treatment cycle
  • Willingness to have an influenza vaccination
  • Signed informed consent

排除标准

  • Any contraindication for flu vaccination
  • Unwillingness to have a flu vaccination
  • Unwillingness to sign informed consent
  • Previous diagnosis of unfavorable endometrial development
  • Unresolved uterine condition that significantly compromises the endometrial cavity

结局指标

主要结局

Clinical Pregnancy

时间窗: 8 weeks

Intrauterine pregnancy with positive evidence of fetal heart beat

次要结局

  • Evidence of immune activation(14 to 21 days (at time of egg retrieval))
  • Implantation Rate(8 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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