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Uterus Transplantation From Live Donors and From Deceased Donors - Clinical Study (UTxLD/DBD)

Primary Purpose

Mayer Rokitansky Kuster Hauser Syndrome, Mullerian Aplasia, Uterus; Absence, Congenital

Status
Recruiting
Phase
Phase 3
Locations
Czechia
Study Type
Interventional
Intervention
Live donor uterus transplantation
Deceased donor uterus transplantation
Tacrolimus
Sponsored by
Institute for Clinical and Experimental Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mayer Rokitansky Kuster Hauser Syndrome focused on measuring uterus transplantation, absolute uterine factor infertility

Eligibility Criteria

18 Years - 60 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria for UTx recipient:

  • 18 - 40 years of age
  • good general health
  • congenital or acquired uterus absence
  • desire for a child

Exclusion Criteria for UTx recipient:

  • age over 40
  • serious comorbidity

Inclusion Criteria for a live uterus donor:

  • female
  • 18 - 60 years of age
  • maximum 4 child births
  • maximum 1 Cesarian section
  • good general health

Exclusion Criteria for a live uterus donor:

  • age over 60
  • hypertension with organ damage
  • diabetes mellitus
  • other serious comorbidity

Inclusion Criteria for a deceased brain-dead uterus donor:

  • female
  • age under 60
  • no previous hysterectomy
  • no previous uterus malignancy

Sites / Locations

  • Institute for Clinical and Experimental MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Live donor uterus transplantation

Deceased donor uterus transplantation

Arm Description

Transplantation of uterus from a living donor. Immunosuppression with tacrolimus.

Transplantation of uterus from a deceased brain-dead donor. Immunosuppression with tacrolimus.

Outcomes

Primary Outcome Measures

Efficacy of uterus transplantation.
Number of successful uterus transplantations and healthy child births. Treatment of absolute uterine factor infertility that has no other therapy option by uterus transplantation that includes in vitro fertilization and cryopreservation, uterus transplantation from a live donor or from a deceased donor, graft survival on immunosuppression, embryo transfer, pregnancy and child birth, final graft hysterectomy.

Secondary Outcome Measures

Comparison of efficacy of uterus transplantation from live donors versus deceased donors.
Number of successful uterus transplantations and healthy child births from live donors versus deceased donors.
Rate of adverse events after uterus transplantation
Number of recipients of uterus transplantation with adverse events.
Rate of adverse events after live uterus donation
Number of live donor participants after uterus retrieval with adverse events.
Rate of adverse events during pregnancy and child birth after uterus transplantation
Number of children conceived and born from transplanted uterus with adverse events.
Verification of technique of uterus retrieval
Verification of surgical technique of uterus retrieval from a live donor and from a deceased donor.

Full Information

First Posted
September 4, 2017
Last Updated
February 25, 2019
Sponsor
Institute for Clinical and Experimental Medicine
Collaborators
University Hospital, Motol, Sahlgrenska University Hospital, Sweden
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1. Study Identification

Unique Protocol Identification Number
NCT03277430
Brief Title
Uterus Transplantation From Live Donors and From Deceased Donors - Clinical Study
Acronym
UTxLD/DBD
Official Title
Uterus Transplantation From Live Donors and From Deceased Donors - Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Recruiting
Study Start Date
October 9, 2015 (Actual)
Primary Completion Date
December 31, 2020 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Institute for Clinical and Experimental Medicine
Collaborators
University Hospital, Motol, Sahlgrenska University Hospital, Sweden

4. Oversight

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

5. Study Description

Brief Summary
Uterus transplantation (UTx) is the only causative treatment for congenital or acquired uterus absence. Individual cases of UTx from a live donor (LD UTx) with healthy child birth performed so far showed favourable outcomes. The present study will include both LD UTx and UTx from deceased donors after brain death (DBD UTx). The aim is treatment of uterine infertility by UTx. It is is an ethically justifiable life-promoting transplantation. Twenty UTx will be performed in 2 parallel arms: 10 LD UTx and 10 DBD UTx. Immunosuppression will be administered. Phases of the UTx procedure are: in vitro fertilization - cryopreservation of embryos - uterus retrieval - UTx - follow up - embryo transfer - pregnancy - child birth - later graft hysterectomy - life long follow up. Introduction of UTx into clinical practice may enable women with uterine infertility to have their own children.
Detailed Description
Introduction: Uterus transplantation (UTx) is the only causative treatment for congenital or acquired uterus absence, i.e. absolute uterine factor infertility (AUFI). Feasibility of uterus transplantation from o live donor and possibility of healthy child birth have been proven in previous clinical study in Sweden. The present study is supposed to extend the swedish experience by including UTx from both live donors and from deceased donors after brain death. Aim: Treatment of absolute uterine factor infertility that has no other therapy option by uterus transplantation. Extending basic knowledge on UTx. Possible introduction of UTx into clinical practice. Indications: UTx can be offered to patients with congenital uterus absence - aplasia uteri et vaginae, also called Mullerian aplasia or Rokitansky-Mayer-Kuster-Hauser syndrome (RMKH), in whom previous neo-vagina was created. UTx can be performed also in women with acquired uterus absence on the basis of previous hysterectomy e.g. for myomas, endometriosis, post-partum bleeding, cervical cancer, uterus malformations or intrauterine adhesions. Ovarian function must be preserved and stable male partner is required for in vitro fertilization (IVF). Ethics: Uterus retrieval from a deceased brain-dead donor does not endanger retrieval of other life-saving organs. Live donor does not loose a vitally important organ. The only alternative is adoption of a child. Surrogacy is illegal in many european countries. UTx is the only causative treatment of AUFI. It is is an ethically justifiable life-promoting transplantation. UTx improves quality of live of both the recipient and the live donor by giving an opportunity to have an own child. Board certification for this study was obtained from the Ministry of Health of the Czech Republic and from the local Ethics Committee. Methods: Twenty UTx will be performed in total in 2 parallel arms: 10 UTx from a live donor (LD UTx) and 10 UTx from a deceased brain-dead donor (DBD UTx). Patients who have no suitable live donor will be wait-listed for a deceased donor. Compatible blood group and negative cross-match test is required. AB0 incompatible or pair exchange transplantations are also possible. Donors and recipients will be examined by clinical, laboratory and imaging methods. All diagnostic and therapeutic procedures will be performed according to a protocol. Risk and benefit will be assessed by a multi-disciplinary team. Informed consent will be signed. Time period between UTx and embryo transfer is supposed to be about 1 year depending on condition of the recipient and the graft, e.g. level of immunosuppression, rejection or infection episodes. Adverse events will be monitored and addressed. Number of possible pregnancies and child births is estimated to be up to 2. The uterus graft will be removed in the end. Overall time interval of keeping the uterus graft in situ and exposure to immunosuppressive therapy is estimated to be up to 5 years. Immunosuppression: Induction immunosuppression is based on thymoglobuline and corticosteroids. Maintenance immunosuppression is based on tacrolimus, mycophenolate and corticosteroids. Temporary anti-infective prophylaxis will be administered. Minimalization of immunosuppression is needed before pregnancy (monotherapy with tacrolimus). Protocol cervix biopsies to look for possible rejection will be performed. Immunosuppression will be discontinued after graft hysterectomy. Phases of the UTx procedure: in vitro fertilization (IVF phase I) - cryopreservation of embryos - uterus retrieval from a live donor or from a deceased donor - orthotopic uterus transplantation with open technique - follow up period - embryo transfer (IVF phase II) - pregnancy - child birth via Cesarian section - later graft hysterectomy - life long follow up. Merit: Individual cases of uterus transplantation performed so far showed favourable outcomes. Introduction of UTx into clinical practice may enable women with uterine infertility to have their own children.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mayer Rokitansky Kuster Hauser Syndrome, Mullerian Aplasia, Uterus; Absence, Congenital, Infertility, Female, Uterus Absence, Acquired, Absolute Uterine Factor Infertility
Keywords
uterus transplantation, absolute uterine factor infertility

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Live donor uterus transplantation
Arm Type
Experimental
Arm Description
Transplantation of uterus from a living donor. Immunosuppression with tacrolimus.
Arm Title
Deceased donor uterus transplantation
Arm Type
Experimental
Arm Description
Transplantation of uterus from a deceased brain-dead donor. Immunosuppression with tacrolimus.
Intervention Type
Procedure
Intervention Name(s)
Live donor uterus transplantation
Intervention Description
Transplantation of uterus from a living donor.
Intervention Type
Procedure
Intervention Name(s)
Deceased donor uterus transplantation
Intervention Description
Transplantation of uterus from a deceased brain-dead donor.
Intervention Type
Drug
Intervention Name(s)
Tacrolimus
Other Intervention Name(s)
FK506
Intervention Description
Maintenance immunosuppression in UTx recipient will be reduced to tacrolimus monotherapy to minimalize fetal compromise.
Primary Outcome Measure Information:
Title
Efficacy of uterus transplantation.
Description
Number of successful uterus transplantations and healthy child births. Treatment of absolute uterine factor infertility that has no other therapy option by uterus transplantation that includes in vitro fertilization and cryopreservation, uterus transplantation from a live donor or from a deceased donor, graft survival on immunosuppression, embryo transfer, pregnancy and child birth, final graft hysterectomy.
Time Frame
Until 10 live donor and 10 deceased donor uterus transplants have been performed plus approximately 5 years.
Secondary Outcome Measure Information:
Title
Comparison of efficacy of uterus transplantation from live donors versus deceased donors.
Description
Number of successful uterus transplantations and healthy child births from live donors versus deceased donors.
Time Frame
Until 10 live donor and 10 deceased donor uterus transplants have been performed plus approximately 5 years.
Title
Rate of adverse events after uterus transplantation
Description
Number of recipients of uterus transplantation with adverse events.
Time Frame
Until 10 live donor and 10 deceased donor uterus transplants have been performed plus approximately 5 years.
Title
Rate of adverse events after live uterus donation
Description
Number of live donor participants after uterus retrieval with adverse events.
Time Frame
Until 10 live donor transplants have been performed plus approximately 5 years.
Title
Rate of adverse events during pregnancy and child birth after uterus transplantation
Description
Number of children conceived and born from transplanted uterus with adverse events.
Time Frame
Until 10 live donor and 10 deceased donor uterus transplants have been performed plus approximately 5 years.
Title
Verification of technique of uterus retrieval
Description
Verification of surgical technique of uterus retrieval from a live donor and from a deceased donor.
Time Frame
Until 10 live donor and 10 deceased donor uterus transplants have been performed plus approximately 5 years.

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria for UTx recipient: 18 - 40 years of age good general health congenital or acquired uterus absence desire for a child Exclusion Criteria for UTx recipient: age over 40 serious comorbidity Inclusion Criteria for a live uterus donor: female 18 - 60 years of age maximum 4 child births maximum 1 Cesarian section good general health Exclusion Criteria for a live uterus donor: age over 60 hypertension with organ damage diabetes mellitus other serious comorbidity Inclusion Criteria for a deceased brain-dead uterus donor: female age under 60 no previous hysterectomy no previous uterus malignancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiri Fronek, Assoc Prof
Phone
+420 26 136 4105
Email
jifr@ikem.cz
First Name & Middle Initial & Last Name or Official Title & Degree
Renata Zamecnikova, Bc
Phone
+420 26 136 4105, 5300
Email
zamr@ikem.cz
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiri Fronek, Assoc Prof
Organizational Affiliation
Transplant Surgery Department, Institute of Clinical and Experimental Medicine, Prague, Czech Republic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute for Clinical and Experimental Medicine
City
Prague
ZIP/Postal Code
14021
Country
Czechia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jiri Fronek, Assoc Prof
Phone
+420 26 136 4105
Email
jifr@ikem.cz
First Name & Middle Initial & Last Name & Degree
Renata Zamecnikova, Bc
Phone
+420 26 136 4105
Email
zamr@ikem.cz
First Name & Middle Initial & Last Name & Degree
Jiri Fronek, Assoc Prof
First Name & Middle Initial & Last Name & Degree
Roman Chmel, MD PhD
First Name & Middle Initial & Last Name & Degree
Michael Olausson, Prof

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
25226847
Citation
Erman Akar M, Ozekinci M, Alper O, Demir D, Cevikol C, Meric Bilekdemir A, Daloglu A, Ongut G, Senol Y, Ozdem S, Uzun G, Luleci G, Suleymanlar G. Assessment of women who applied for the uterine transplant project as potential candidates for uterus transplantation. J Obstet Gynaecol Res. 2015 Jan;41(1):12-6. doi: 10.1111/jog.12486. Epub 2014 Sep 17.
Results Reference
background
PubMed Identifier
24784936
Citation
Olausson M, Johannesson L, Brattgard D, Diaz-Garcia C, Lundmark C, Groth K, Marcickiewizc J, Enskog A, Akouri R, Tzakis A, Rogiers X, Janson PO, Brannstrom M. Ethics of uterus transplantation with live donors. Fertil Steril. 2014 Jul;102(1):40-3. doi: 10.1016/j.fertnstert.2014.03.048. Epub 2014 Apr 28. No abstract available.
Results Reference
background
PubMed Identifier
25259905
Citation
Johannesson L, Dahm-Kahler P, Eklind S, Brannstrom M. The future of human uterus transplantation. Womens Health (Lond). 2014 Jul;10(4):455-67. doi: 10.2217/whe.14.22.
Results Reference
background
PubMed Identifier
24726215
Citation
Farrell RM, Falcone T. Uterine transplantation. Fertil Steril. 2014 May;101(5):1244-5. doi: 10.1016/j.fertnstert.2014.03.022. Epub 2014 Apr 13. No abstract available.
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
PubMed Identifier
24535028
Citation
Ozturk H. How real is the uterine transplantation? Ann Transplant. 2014 Feb 14;19:82-3. doi: 10.12659/AOT.889973. No abstract available.
Results Reference
background
PubMed Identifier
24992779
Citation
Akar ME, Ozkan O, Ozekinci M, Sindel M, Yildirim F, Oguz N. Uterus retrieval in cadaver: technical aspects. Clin Exp Obstet Gynecol. 2014;41(3):293-5.
Results Reference
background
PubMed Identifier
32541565
Citation
Fronek J, Janousek L, Kristek J, Chlupac J, Pluta M, Novotny R, Maluskova J, Olausson M. Live Birth Following Uterine Transplantation From a Nulliparous Deceased Donor. Transplantation. 2021 May 1;105(5):1077-1081. doi: 10.1097/TP.0000000000003346.
Results Reference
derived
Links:
URL
http://www.ikem.cz/en/transplantcentrum/klinika-transplantacni-chirurgie/o-nas/programy/transplantace-delohy/a-2460/
Description
Uterine transplantation in the Czech Republic, description and contacts

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Uterus Transplantation From Live Donors and From Deceased Donors - Clinical Study

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