search
Back to results

Uterine Transplant in Absolute Uterine Infertility (AUIF)

Primary Purpose

Female Infertility

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Uterine Transplant
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Female Infertility focused on measuring Infertility, AUFI

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Uterine Transplant Inclusion/Exclusion Criteria

RECIPIENT:Inclusion Criteria

  • Age 18-40
  • Clinical evidence of AUFI (Absolute Uterine Factor Infertility)
  • Able to produce at least 6 normal embryos by IVF for future use
  • Reasonable weight with BMI (Body Mass Index) less than 30.
  • Normal kidney function
  • Able to undergo transplant and be compliant with treatment
  • Has stable partner and social supports
  • 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 comply with required treatment (taking pills, having biopsies, frequent appointments )
  • Having a condition that would make pregnancy or taking anti rejection medicines too risky.
  • Active infection: Human Immunodeficiency Virus (HIV) , Tuberculosis, Hepatitis B, Hepatitis C
  • History of extensive abdominal or pelvic surgery
  • History of abnormal Papanicolaou test (PAP smear) or genital warts
  • History of pelvic inflammatory disease

DONOR:Inclusion criteria

  • Age over 40 up to age 60
  • Has completed having a family
  • Previous pregnancies were carried to term (no miscarriages)
  • Able to take a birth control pill containing estrogen
  • Weight reasonable with BMI (Body Mass Index) of 30 or less
  • Good social supports

Exclusion Criteria:

  • Active smoking, alcohol use or use of illicit drugs
  • Psychiatric illness
  • Cervical or endometrial polyps (growths) or tumors in the uterus muscle
  • History of more than 1 Caesarean section
  • History of abnormal PAP smear or genital warts
  • Internal scarring from extensive abdominal or pelvic surgery
  • Hypertension, Coronary artery disease, Chronic Obstructive Lung disease (emphysema) and Diabetes
  • Active cancer or incompletely treated cancer
  • Active infection including Human Immunodeficiency Disease (HIV) , Tuberculosis, Hepatitis B or Hepatitis C
  • Significant history of either blood clots or bleeding tendencies
  • Evidence of coercion or exchange of money or goods for donating the organ

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Women with AUFI

    Arm Description

    Women with AUFI must meet criteria for uterine transplant. In vitro fertilization to obtain 6 (screened) healthy embryos for cryo-preservation precedes uterine transplant from an appropriate donor The recipient will be required to take potent anti rejection medications including Thymoglobulin, Prednisone, Tacrolimus, Mycophenolate Mofetil (MMF) , later substituted with Azathioprine to avoid birth defects. One year later, up to 6 attempts using 1 screened embryo at a time will be tried to achieve pregnancy. During pregnancy, the high risk pregnancy and transplant teams will follow the recipient. The goal is a full term baby and delivery will be by Caesarian section. A second pregnancy may be attempted. Afterward, the uterus will be explanted.

    Outcomes

    Primary Outcome Measures

    Number of successful live births following uterus transplant/embryo transfer
    Full term live birth by caesarian section after uterus transplant and IVF

    Secondary Outcome Measures

    Rate of complications during pregnancy in uterus transplant recipient
    Monitoring for pre-eclampsia, hypertension, pre-term delivery
    Rate of complications following uterine donation
    Monitoring for excessive bleeding , infection and bladder dysfunction
    Impact of uterine donation on donor quality of life
    Measured by serial SF 36 QOL survey by psychiatrist at pre-donation and at follow-up appointments
    Cost comparison for uterine transplant vs. surrogacy vs adoption
    At the end of the study, investigators will calculate average cost of each modality, i.e. transplant vs surrogacy vs adoption to compare the three alternatives to infertility
    Impact of uterine transplant on quality of life
    Measured by serial SF 36 QOL survey by psychiatrist pre-transplant and at follow-up appointments..

    Full Information

    First Posted
    February 22, 2016
    Last Updated
    April 27, 2016
    Sponsor
    Brigham and Women's Hospital
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT02741102
    Brief Title
    Uterine Transplant in Absolute Uterine Infertility (AUIF)
    Official Title
    Uterine Transplant in Absolute Uterine Infertility (AUIF)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    June 2016 (undefined)
    Primary Completion Date
    June 2022 (Anticipated)
    Study Completion Date
    January 2023 (Anticipated)

    3. Sponsor/Collaborators

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

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This study will examine the feasibility of initiating a uterine transplant program for Absolute Uterine Factor Infertility (AUFI) at Brigham and Women's Hospital. The investigators plan to screen 30 patients with a goal of enrolling 10 patients. (5 donors and 5 recipients) After careful screening, appropriate candidates will undergo IVF, Uterine Transplantation, Embryo Transfer, Pregnancy and Delivery. Once the uterus is explanted, five years of follow-up is planned.
    Detailed Description
    There are approximately 9.5 million women in the United States with Absolute Uterine Factor Infertility (AUFI).Congenital uterine infertility in women is linked to a malformed or absent mullerian system termed MRKH - Rokitansky's or Mayer-Rokitansky-Kuster-Hauser Syndrome). Additional causes of acquired uterine infertility include a hysterectomy subsequent to life-threatening hemorrhage during childbirth or as a consequence to a hysterectomy related to cervical cancer or for large symptomatic fibroids. Additional causes may include intrauterine adhesions subsequent to surgical abortion or infection. Uterine transplantation will provide a much needed medical option for many women in the U.S. and overseas who are unable to carry their own children based on uterine infertility. Centers outside of the US have initiated uterus transplant programs. Initial attempts were reported from Saudi Arabia. While the deceased donor transplant had been successful, successful pregnancies were not achieved. Another deceased donor transplant had been performed in Turkey with a uterus procured from a deceased donor. Although several IVF attempts had been performed, they had not resulted in live births. Uterus transplants from live donors have been successful. In October 2014, Swedish doctors treating a woman born without a uterus, announced the world's first live birth of a healthy baby boy after a live donor uterine transplantation. Since then, an additional three babies have been born in Sweden to mothers who received live donor uterus transplants. A fifth baby is at term and a 6th pregnancy has been reported. For this study, the investigators plan to screen 30 patients in order to enroll 10 patients, 5 recipients and their respective donors. Prospective recipients will undergo comprehensive medical and psychological evaluation. If deemed an appropriate candidate, In Vitro Fertilization would be started with the goal of obtaining 6 normal embryos for implantation. The uterus of a suitable live donor would then transplanted into the recipient. The recipient would need to take potent anti-rejection drugs and undergo regular assessments for rejection. After one year, embryo transfer to the transplanted uterus would be tried. Up to 6 cycles would be attempted hopefully resulting in pregnancy. If pregnancy results, the recipient would be followed by the high risk pregnancy team. Delivery will be by Caesarian Section. A woman may have up to 2 pregnancies with the transplanted uterus. The uterus is later removed so the recipient no longer has to take anti-rejection drugs.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Female Infertility
    Keywords
    Infertility, 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
    10 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Women with AUFI
    Arm Type
    Experimental
    Arm Description
    Women with AUFI must meet criteria for uterine transplant. In vitro fertilization to obtain 6 (screened) healthy embryos for cryo-preservation precedes uterine transplant from an appropriate donor The recipient will be required to take potent anti rejection medications including Thymoglobulin, Prednisone, Tacrolimus, Mycophenolate Mofetil (MMF) , later substituted with Azathioprine to avoid birth defects. One year later, up to 6 attempts using 1 screened embryo at a time will be tried to achieve pregnancy. During pregnancy, the high risk pregnancy and transplant teams will follow the recipient. The goal is a full term baby and delivery will be by Caesarian section. A second pregnancy may be attempted. Afterward, the uterus will be explanted.
    Intervention Type
    Procedure
    Intervention Name(s)
    Uterine Transplant
    Intervention Description
    Treating Absolute Uterine Factor Infertility by Uterus Transplant. Potential recipients undergo IVF to obtain 6 embryos for cryopreservation followed by live donor uterine transplant. After 1 year, embryo transfer is done to achieve pregnancy. Delivery is by Caesarian section. The recipient may have up to 2 children by these methods and then the uterus is removed so that immunosuppression can be stopped.
    Primary Outcome Measure Information:
    Title
    Number of successful live births following uterus transplant/embryo transfer
    Description
    Full term live birth by caesarian section after uterus transplant and IVF
    Time Frame
    2 years after uterine transplant
    Secondary Outcome Measure Information:
    Title
    Rate of complications during pregnancy in uterus transplant recipient
    Description
    Monitoring for pre-eclampsia, hypertension, pre-term delivery
    Time Frame
    9 months after pregnancy achieved by embryo transfer
    Title
    Rate of complications following uterine donation
    Description
    Monitoring for excessive bleeding , infection and bladder dysfunction
    Time Frame
    Up to 2 years post donation
    Title
    Impact of uterine donation on donor quality of life
    Description
    Measured by serial SF 36 QOL survey by psychiatrist at pre-donation and at follow-up appointments
    Time Frame
    Up to 2 years post donation
    Title
    Cost comparison for uterine transplant vs. surrogacy vs adoption
    Description
    At the end of the study, investigators will calculate average cost of each modality, i.e. transplant vs surrogacy vs adoption to compare the three alternatives to infertility
    Time Frame
    Up to 5 years after uterine transplant
    Title
    Impact of uterine transplant on quality of life
    Description
    Measured by serial SF 36 QOL survey by psychiatrist pre-transplant and at follow-up appointments..
    Time Frame
    Up to 5 years after uterine transplant

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Uterine Transplant Inclusion/Exclusion Criteria RECIPIENT:Inclusion Criteria Age 18-40 Clinical evidence of AUFI (Absolute Uterine Factor Infertility) Able to produce at least 6 normal embryos by IVF for future use Reasonable weight with BMI (Body Mass Index) less than 30. Normal kidney function Able to undergo transplant and be compliant with treatment Has stable partner and social supports 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 comply with required treatment (taking pills, having biopsies, frequent appointments ) Having a condition that would make pregnancy or taking anti rejection medicines too risky. Active infection: Human Immunodeficiency Virus (HIV) , Tuberculosis, Hepatitis B, Hepatitis C History of extensive abdominal or pelvic surgery History of abnormal Papanicolaou test (PAP smear) or genital warts History of pelvic inflammatory disease DONOR:Inclusion criteria Age over 40 up to age 60 Has completed having a family Previous pregnancies were carried to term (no miscarriages) Able to take a birth control pill containing estrogen Weight reasonable with BMI (Body Mass Index) of 30 or less Good social supports Exclusion Criteria: Active smoking, alcohol use or use of illicit drugs Psychiatric illness Cervical or endometrial polyps (growths) or tumors in the uterus muscle History of more than 1 Caesarean section History of abnormal PAP smear or genital warts Internal scarring from extensive abdominal or pelvic surgery Hypertension, Coronary artery disease, Chronic Obstructive Lung disease (emphysema) and Diabetes Active cancer or incompletely treated cancer Active infection including Human Immunodeficiency Disease (HIV) , Tuberculosis, Hepatitis B or Hepatitis C Significant history of either blood clots or bleeding tendencies Evidence of coercion or exchange of money or goods for donating the organ
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Stefan G Tullius, M.D.
    Phone
    617-732-6866
    Email
    stullius@partners.org
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Stefan G Tullius, M.D.
    Organizational Affiliation
    Brigham and Womens Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    9747668
    Citation
    Armenti VT, Moritz MJ, Davison JM. Drug safety issues in pregnancy following transplantation and immunosuppression: effects and outcomes. Drug Saf. 1998 Sep;19(3):219-32. doi: 10.2165/00002018-199819030-00005.
    Results Reference
    background
    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
    Citation
    Christensen, M, Kronberg, CJ, Knudsen UB: Pre-eclampsia and arterial stiffness - a 10 year follow-up of previous pre-eclamptic women. Pregnancy Hyprtens 2015; 5: 72-73.
    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
    23978550
    Citation
    Josephson MA, McKay DB. Women and transplantation: fertility, sexuality, pregnancy, contraception. Adv Chronic Kidney Dis. 2013 Sep;20(5):433-40. doi: 10.1053/j.ackd.2013.06.005. Erratum In: Adv Chronic Kidney Dis. 2014 Jan;21(1):114.
    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
    15121619
    Citation
    Le Ray C, Coulomb A, Elefant E, Frydman R, Audibert F. Mycophenolate mofetil in pregnancy after renal transplantation: a case of major fetal malformations. Obstet Gynecol. 2004 May;103(5 Pt 2):1091-4. doi: 10.1097/01.AOG.0000124986.32858.ba.
    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
    PubMed Identifier
    19897849
    Citation
    Brannstrom M, Wranning CA, Altchek A. Experimental uterus transplantation. Hum Reprod Update. 2010 May-Jun;16(3):329-45. doi: 10.1093/humupd/dmp049. Epub 2009 Nov 7.
    Results Reference
    background
    PubMed Identifier
    6132996
    Citation
    Szekeres-Bartho J, Csernus V, Hadnagy J, Pacsa AS. Immunosuppressive effect of serum progesterone during pregnancy depends on the progesterone binding capacity of the lymphocytes. J Reprod Immunol. 1983 Mar;5(2):81-8. doi: 10.1016/0165-0378(83)90003-7.
    Results Reference
    background
    PubMed Identifier
    26088636
    Citation
    Balayla J, Dahdouh EM, Lefkowitz A; Montreal Criteria for the Ethical Feasibility of Uterine Transplantation Research Group. Livebirth after uterus transplantation. Lancet. 2015 Jun 13;385(9985):2351-2. doi: 10.1016/S0140-6736(15)61096-0. No abstract available.
    Results Reference
    result

    Learn more about this trial

    Uterine Transplant in Absolute Uterine Infertility (AUIF)

    We'll reach out to this number within 24 hrs