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
About this trial
This is an interventional treatment trial for Infertility of Uterine Origin focused on measuring AUFI
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
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
NCT ID
NCT04026893
First Posted
May 2, 2019
Last Updated
July 18, 2019
Sponsor
Brigham and Women's Hospital
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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