Effect of Influenza Vaccination on Donor Egg Recipient Outcomes (DE-FluVac)
Primary Purpose
Infertility, Recurrent Miscarriage
Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Influenza Vaccine
Sterile Saline
Sponsored by
About this trial
This is an interventional treatment trial for Infertility focused on measuring Immunology, Pregnancy, Implantation Rate, Fertilization in Vitro, Oocyte donor egg recipient
Eligibility Criteria
Inclusion Criteria:
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
Exclusion Criteria:
- 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
Sites / Locations
- Center For Human Reproduction
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Influenza Vaccine
Saline Injection
Arm Description
O.5 mL single dose influenza vaccine suspension administered intramuscularly
O.5 ml of sterile Saline administered intramuscularly
Outcomes
Primary Outcome Measures
Clinical Pregnancy
Intrauterine pregnancy with positive evidence of fetal heart beat
Secondary Outcome Measures
Implantation Rate
Number of clinical pregnancies per number of embryos transferred
Evidence of immune activation
Evidence of peripheral markers of immune pathways activated by the influenza vaccine
Full Information
NCT ID
NCT02946177
First Posted
October 25, 2016
Last Updated
February 15, 2020
Sponsor
Center for Human Reproduction
Collaborators
Foundation for Human Reproduction
1. Study Identification
Unique Protocol Identification Number
NCT02946177
Brief Title
Effect of Influenza Vaccination on Donor Egg Recipient Outcomes
Acronym
DE-FluVac
Official Title
A Randomized Controlled Trial of the Effect of Influenza Vaccination on Implantation and Pregnancy Rates After Donor Egg Recipient In-Vitro Fertilization
Study Type
Interventional
2. Study Status
Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 19, 2017 (Actual)
Primary Completion Date
December 31, 2020 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Center for Human Reproduction
Collaborators
Foundation for Human Reproduction
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed Description
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:
History of recurrent miscarriage or implantation failure
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Recurrent Miscarriage
Keywords
Immunology, Pregnancy, Implantation Rate, Fertilization in Vitro, Oocyte donor egg recipient
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
126 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Influenza Vaccine
Arm Type
Experimental
Arm Description
O.5 mL single dose influenza vaccine suspension administered intramuscularly
Arm Title
Saline Injection
Arm Type
Placebo Comparator
Arm Description
O.5 ml of sterile Saline administered intramuscularly
Intervention Type
Biological
Intervention Name(s)
Influenza Vaccine
Other Intervention Name(s)
Seqirus afluria 2016-2017 formula
Intervention Description
Inactivated influenza vaccine indicated for immunization against disease caused by influenza virus subtype A and type B present in the vaccine. Approved for use in persons 5 years of age and older. Single Dose prefilled 0.5 ml syringe.
Intervention Type
Other
Intervention Name(s)
Sterile Saline
Other Intervention Name(s)
Saline
Intervention Description
0.5 mL of sterile Saline administered im
Primary Outcome Measure Information:
Title
Clinical Pregnancy
Description
Intrauterine pregnancy with positive evidence of fetal heart beat
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Implantation Rate
Description
Number of clinical pregnancies per number of embryos transferred
Time Frame
8 weeks
Title
Evidence of immune activation
Description
Evidence of peripheral markers of immune pathways activated by the influenza vaccine
Time Frame
14 to 21 days (at time of egg retrieval)
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
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
Exclusion Criteria:
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David H Barad, MD, MS
Organizational Affiliation
Director of Assisted Reproductive Technology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Norbert Gleicher, MD
Organizational Affiliation
Medical Director
Official's Role
Study Director
Facility Information:
Facility Name
Center For Human Reproduction
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
We do not plan to share individual participant data (IPD)
Learn more about this trial
Effect of Influenza Vaccination on Donor Egg Recipient Outcomes
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