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Deceased Uterine Transplant in Absolute Uterine Infertility (AUIF)

Primary Purpose

Infertility of Uterine Origin

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Uterine Transplant from Deceased Donor
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility of Uterine Origin focused on measuring AUFI

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Evidence of AUFI diagnosed by BWH gynecologist
  • Ability to produce at least 6 euploid embryos for cryopreservation
  • BMI ≤ 30
  • GFR 60 or greater in any patient including those with a single kidney
  • PRA 20% or less
  • Deemed stable and capable of undergoing transplant by the transplant team to include psychiatry, social work, and transplant coordinator and study doctors to assure compliance with treatment
  • Evidence to be compliant with follow-up and immunosuppression
  • Partner willing to undergo psychological evaluation and receive immunizations as recommended
  • Stable home environment to support a child

Exclusion Criteria:

  • Active smoking, alcohol use or use of illicit drugs
  • Inability to follow a strict medication dosing schedule post-transplant and adhere to required follow-up appointments.
  • Any co-morbidities which would increase surgical risk, risk of pregnancy or the risk of taking anti-rejection medications as determined by the Maternal Fetal Specialist and Transplant Surgeon.
  • Active infection: HIV, Hepatitis B, Hepatitis C
  • Inadequate blood vessels to support the transplanted uterus.
  • Prior extensive abdominal or pelvic surgery
  • Presence of pelvic kidney
  • History of abnormal PAP
  • HPV related vulvar, vaginal or cervical dysplasia
  • Evidence of genital condylomata
  • History of PID
  • One or more living biological children

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Number of Live Births Following Uterus Transplant
    To provide motherhood options for women with AUIF as an alternative to surrogacy or adoption, via gestating and giving birth via Cesarean section to a live infant.
    Number of Surgically Successful Uterus Transplants
    To achieve surgically successful uterus transplants.

    Secondary Outcome Measures

    Financial impact of deceased donor uterus transplantation
    To analyze the overall impact of deceased donor uterus transplantation costs relative to established alternative procedures such as adoption and surrogacy.
    Quality of life impact of deceased donor uterus transplantation
    To analyze the overall impact of deceased donor uterus transplantation including changes in quality of life, relative to other established alternative procedures such as adoption and surrogacy.

    Full Information

    First Posted
    May 2, 2019
    Last Updated
    July 18, 2019
    Sponsor
    Brigham and Women's Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04026893
    Brief Title
    Deceased Uterine Transplant in Absolute Uterine Infertility (AUIF)
    Official Title
    Deceased Uterine Transplant in Absolute Uterine Infertility (AUIF)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2019
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2020 (Anticipated)
    Primary Completion Date
    September 1, 2025 (Anticipated)
    Study Completion Date
    October 1, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Brigham and Women's Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Our study will explore the feasibility of initiating a deceased donor uterine transplant program in addition to the existing living donor IRB at BWH. Using the template established by teams around the world, we will identify emotionally and socially stable females of reproductive age with intact ovaries who are unable to gestate a child due to congenital or acquired uterine factor infertility. After careful screening, participants will undergo egg harvest, in vitro fertilization, and embryo cryopreservation using standard methods. Women who successfully complete the fertilization of at least six euploid embryos will be eligible to be placed on the waitlist for a deceased donor uterus transplant. After a successful transplant and a period of observation to ensure normal menstrual cycle and graft viability (anticipate six months), embryo implantation will be undertaken. Following an embryo transfer, gestation will be carefully monitored by our high-risk pregnancy specialists. Medical research interventions include the surgical implantation of a uterus utilizing techniques by teams that have applied this approach successfully, close post-transplant follow up including immunosuppression therapy tailored to established standards during pregnancy minimizing fetal risks, and careful management of pregnancy. After childbearing is complete (at most two gestations), the donor uterus will be removed either during Cesarean or during an elective procedure. In addition, open ended interviews and surveys will be conducted to elicit ethical and psychosocial concerns arising from the experience of subjects and their families, health care providers, and the wider community. The investigator's intent is to monitor outcomes for transplant recipients as well as the live born infants for 30 days after removal of the transplanted uterus. It is estimated that the time from screening to a potential live birth will be a minimum of 22 months, but likely between 24 - 36 months depending on organ availability.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Infertility of Uterine Origin
    Keywords
    AUFI

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    250 (Anticipated)

    8. Arms, Groups, and Interventions

    Intervention Type
    Procedure
    Intervention Name(s)
    Uterine Transplant from Deceased Donor
    Intervention Description
    The recipient will be started on anti-rejection medications (as is routine for transplant recipients) prior to the OR. Standard of care anesthesia and line placement will take place. The recipient will be appropriately identified as an organ recipient and the donor organ identified per required transplant protocols already in place. The recipient team will then connect the vasculature and appropriate supporting structures for the uterus transplant. Once the organ has been re-perfused, the remainder of the operation will take place and the patient will be moved to the Intensive Care Unit and later to the transplant patient floor for standard monitoring.
    Primary Outcome Measure Information:
    Title
    Number of Live Births Following Uterus Transplant
    Description
    To provide motherhood options for women with AUIF as an alternative to surrogacy or adoption, via gestating and giving birth via Cesarean section to a live infant.
    Time Frame
    Within 5 years of transplant
    Title
    Number of Surgically Successful Uterus Transplants
    Description
    To achieve surgically successful uterus transplants.
    Time Frame
    Within 3 months of transplant
    Secondary Outcome Measure Information:
    Title
    Financial impact of deceased donor uterus transplantation
    Description
    To analyze the overall impact of deceased donor uterus transplantation costs relative to established alternative procedures such as adoption and surrogacy.
    Time Frame
    Through Study completion, up to 5 years post transplant
    Title
    Quality of life impact of deceased donor uterus transplantation
    Description
    To analyze the overall impact of deceased donor uterus transplantation including changes in quality of life, relative to other established alternative procedures such as adoption and surrogacy.
    Time Frame
    Through study completion, up to 5 years post transplant

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Evidence of AUFI diagnosed by BWH gynecologist Ability to produce at least 6 euploid embryos for cryopreservation BMI ≤ 30 GFR 60 or greater in any patient including those with a single kidney PRA 20% or less Deemed stable and capable of undergoing transplant by the transplant team to include psychiatry, social work, and transplant coordinator and study doctors to assure compliance with treatment Evidence to be compliant with follow-up and immunosuppression Partner willing to undergo psychological evaluation and receive immunizations as recommended Stable home environment to support a child Exclusion Criteria: Active smoking, alcohol use or use of illicit drugs Inability to follow a strict medication dosing schedule post-transplant and adhere to required follow-up appointments. Any co-morbidities which would increase surgical risk, risk of pregnancy or the risk of taking anti-rejection medications as determined by the Maternal Fetal Specialist and Transplant Surgeon. Active infection: HIV, Hepatitis B, Hepatitis C Inadequate blood vessels to support the transplanted uterus. Prior extensive abdominal or pelvic surgery Presence of pelvic kidney History of abnormal PAP HPV related vulvar, vaginal or cervical dysplasia Evidence of genital condylomata History of PID One or more living biological children
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Stefan G Tullius, MD
    Phone
    617-732-6866
    Email
    stullius@bwh.harvard.edu
    First Name & Middle Initial & Last Name or Official Title & Degree
    Shannon Weiss
    Phone
    617-525-9763
    Email
    sweiss3@bwh.harvard.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Stefan G Tullius, MD
    Organizational Affiliation
    Brigham and Women's Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    Data will be published or presented at scientific meetings or distributed upon request.
    IPD Sharing Time Frame
    For the duration of the study.
    IPD Sharing Access Criteria
    Data will be published or presented at scientific meetings or distributed upon request.
    Citations:
    PubMed Identifier
    24582522
    Citation
    Brannstrom M, Johannesson L, Dahm-Kahler P, Enskog A, Molne J, Kvarnstrom N, Diaz-Garcia C, Hanafy A, Lundmark C, Marcickiewicz J, Gabel M, Groth K, Akouri R, Eklind S, Holgersson J, Tzakis A, Olausson M. First clinical uterus transplantation trial: a six-month report. Fertil Steril. 2014 May;101(5):1228-36. doi: 10.1016/j.fertnstert.2014.02.024. Epub 2014 Feb 27.
    Results Reference
    background
    PubMed Identifier
    22533575
    Citation
    Tullius SG, Rudolf JA, Malek SK. Moving boundaries--the Nightingale twins and transplantation science. N Engl J Med. 2012 Apr 26;366(17):1564-5. doi: 10.1056/NEJMp1114193. No abstract available.
    Results Reference
    background
    PubMed Identifier
    22356169
    Citation
    Lefkowitz A, Edwards M, Balayla J. The Montreal Criteria for the Ethical Feasibility of Uterine Transplantation. Transpl Int. 2012 Apr;25(4):439-47. doi: 10.1111/j.1432-2277.2012.01438.x. Epub 2012 Feb 23.
    Results Reference
    background
    PubMed Identifier
    23202992
    Citation
    Del Priore G, Saso S, Meslin EM, Tzakis A, Brannstrom M, Clarke A, Vianna R, Sawyer R, Smith JR. Uterine transplantation--a real possibility? The Indianapolis consensus. Hum Reprod. 2013 Feb;28(2):288-91. doi: 10.1093/humrep/des406. Epub 2012 Nov 30.
    Results Reference
    background
    PubMed Identifier
    16554530
    Citation
    McKay DB, Josephson MA. Pregnancy in recipients of solid organs--effects on mother and child. N Engl J Med. 2006 Mar 23;354(12):1281-93. doi: 10.1056/NEJMra050431. No abstract available.
    Results Reference
    background

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    Deceased Uterine Transplant in Absolute Uterine Infertility (AUIF)

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