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Autologous Bone Marrow-derived Mesenchymal Stem Cells for Atrophic Endometrium in Patients With Repeated IVF Failures

Primary Purpose

Infertility, Female, Infertility of Uterine Origin, Asherman Syndrome

Status
Completed
Phase
Phase 2
Locations
Russian Federation
Study Type
Interventional
Intervention
bone marrow-derived MSC and HRT
hormonal replacement therapy
Sponsored by
D.O. Ott Research Institute of Obstetrics, Gynecology, and Reproductology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility, Female focused on measuring Repeated IVF failure, Stem cell

Eligibility Criteria

21 Years - 44 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Repeated IVF attempts with high and good quality embryo transfer in fresh and frozen IVF cycles;
  • Age 20-44 years;
  • Endometrial thickness less than 6 mm in 2 or more of HRT cycles for endometrial preparation for embryo transfer
  • Hysteroscopic evidence of fibrosis processes of uterine cavity with the absence of positive dynamics of HRT in 3 months following operation;
  • Signed informed consent.

Exclusion Criteria:

  • Contraindication for pregnancy;
  • Absence of cryopreserved embryos, stored at clinic's cryobank;
  • BMI > 30 kg/m2;
  • Impaired carbohydrate metabolism according to glucose tolerance test;
  • Thrombosis in anamnesis;
  • Oncological diseases in anamnesis;
  • Diagnosed inherited thrombophilia;
  • Uterine fibroids of more than 4 cm or more than 2 fibroids of 2.5 cm diameter;
  • Nodal form of adenomiosis;
  • Ovarian cysts more than 4 cm in diameter.

Sites / Locations

  • D.O. Ott Research Institute of Obstetrics, Gynecology, and Reproductology

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

bone marrow-derived MSC and HRT

hormonal replacement therapy

Arm Description

endometrial injection of autologous cell product of MSC with hormonal replacement therapy before frozen/thawed ET

standard endometrial preparation for frozen/thawed ET

Outcomes

Primary Outcome Measures

Assessment of endometrial receptivity
combination of endometrial thickness on ultrasound and immunohistochemistry of endometrium assessed at the biopsy day of the third cycle of HRT

Secondary Outcome Measures

Clinical pregnancy rate
presence of intrauterine gestational sac at transvaginal ultrasound at 5-6 weeks of gestation or 5-6 weeks after starting the intervention; measured per frozen/thawed embryo transfer
Treatment-Emergent Adverse Events
Incidence of adverse events: side reactions, abdominal discomfort and patient's tolerance (Safety and Tolerability)

Full Information

First Posted
May 23, 2017
Last Updated
December 31, 2019
Sponsor
D.O. Ott Research Institute of Obstetrics, Gynecology, and Reproductology
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1. Study Identification

Unique Protocol Identification Number
NCT03166189
Brief Title
Autologous Bone Marrow-derived Mesenchymal Stem Cells for Atrophic Endometrium in Patients With Repeated IVF Failures
Official Title
Open Randomized Trial of Clinical Efficiency and Safety of Cell Product of Autologous Bone Marrow-derived Mesenchymal Stem Cells for Reparative Treatment of Destructively Changed Endometrium in Patients With Repeated IVF Failures
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Completed
Study Start Date
December 20, 2017 (Actual)
Primary Completion Date
March 16, 2019 (Actual)
Study Completion Date
December 28, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
D.O. Ott Research Institute of Obstetrics, Gynecology, and Reproductology

4. Oversight

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

5. Study Description

Brief Summary
Investigators will examine safety and efficiency of the cell product of autologous bone marrow-derived mesenchymal stem cells (MSC) for patients with repeated IVF failures and hypoplastic or/and fibrosis process of endometrium
Detailed Description
Sixty patients eligible for the study will be divided to two groups (experimental and control) according to randomization (envelope) procedure in 1:1 ratio. For patients of the main group bone marrow stem cells will be extracted from the crest of the ilium using standard methodology. After extraction and cultivation final product of autologous bone marrow-derived mesenchymal stem cells will be transplanted to endometrial cavity on menstrual cycle day 5-6. Meanwhile patients will receive three cycles of hormonal replacement therapy (4 mg Progynova (Bayer Pharma, Germany) daily on menstrual cycle day 5-25 in combination with 20 mg Duphaston (Abbott Healthcare Products, B.V., Netherlands) daily from day 15 to day 25. On day 20 of hormonal replacement therapy (HRT) of the last (third) cycle Pipelle-biopsy of endometrium will be performed. Obtained material will be analyzed by immunohistochemistry with the assessment of estrogen and progesterone receptors, VEGFa, GM-CSF, CD133+, CD34 and CD56. Ultrasound characteristics of endometrial quality will be registered on day 9-10 and day 19-21 of every cycle. When morphological and echographic parameters of endometrium are found satisfactory for embryo transfer, the HRT for endometrial preparation for frozen/thawed embryo transfer cycle will be initiated. If acceptable endometrial characteristics are not achieved, patients could be offered to undergo repeated (not more than 3) transplantation of MSC procedures. Control group will receive three standard cycles of HRT following hysteroscopy before frozen/thawed embryo transfer. If endometrial characteristics are found unsatisfactory, gestational surrogacy might be offered.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Female, Infertility of Uterine Origin, Asherman Syndrome
Keywords
Repeated IVF failure, Stem cell

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
46 (Actual)

8. Arms, Groups, and Interventions

Arm Title
bone marrow-derived MSC and HRT
Arm Type
Experimental
Arm Description
endometrial injection of autologous cell product of MSC with hormonal replacement therapy before frozen/thawed ET
Arm Title
hormonal replacement therapy
Arm Type
Active Comparator
Arm Description
standard endometrial preparation for frozen/thawed ET
Intervention Type
Biological
Intervention Name(s)
bone marrow-derived MSC and HRT
Intervention Description
Transplantation procedure to endometrial cavity is performed with ultrasound guidance on menstrual cycle day 5-6 through uterine cervix using cater for embryo transfer with 1 ml of suspension containing 5 millions of autologous bone marrow-derived mesenchymal stem cells Three cycles of HRT following MSC transplantation; Pipelle-biopsy of endometrium on day 20 of hormonal replacement therapy of the last (third) cycle; Frozen/thawed embryo transfer 3-6 months after transplantation.
Intervention Type
Other
Intervention Name(s)
hormonal replacement therapy
Intervention Description
standard treatment of hypoplastic endometrium or Asherman's syndrome: Three cycles of HRT preceding frozen/thawed embryo transfer; Frozen/thawed embryo transfer.
Primary Outcome Measure Information:
Title
Assessment of endometrial receptivity
Description
combination of endometrial thickness on ultrasound and immunohistochemistry of endometrium assessed at the biopsy day of the third cycle of HRT
Time Frame
3-6 month after randomization
Secondary Outcome Measure Information:
Title
Clinical pregnancy rate
Description
presence of intrauterine gestational sac at transvaginal ultrasound at 5-6 weeks of gestation or 5-6 weeks after starting the intervention; measured per frozen/thawed embryo transfer
Time Frame
3-4 weeks after embryo transfer
Title
Treatment-Emergent Adverse Events
Description
Incidence of adverse events: side reactions, abdominal discomfort and patient's tolerance (Safety and Tolerability)
Time Frame
3-6 month after randomization

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
44 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Repeated IVF attempts with high and good quality embryo transfer in fresh and frozen IVF cycles; Age 20-44 years; Endometrial thickness less than 6 mm in 2 or more of HRT cycles for endometrial preparation for embryo transfer Hysteroscopic evidence of fibrosis processes of uterine cavity with the absence of positive dynamics of HRT in 3 months following operation; Signed informed consent. Exclusion Criteria: Contraindication for pregnancy; Absence of cryopreserved embryos, stored at clinic's cryobank; BMI > 30 kg/m2; Impaired carbohydrate metabolism according to glucose tolerance test; Thrombosis in anamnesis; Oncological diseases in anamnesis; Diagnosed inherited thrombophilia; Uterine fibroids of more than 4 cm or more than 2 fibroids of 2.5 cm diameter; Nodal form of adenomiosis; Ovarian cysts more than 4 cm in diameter.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexandr Gzgzyan, Prof, PhD
Organizational Affiliation
D.O. Ott Research Institute of Obstetrics, Gynecology, and Reproductology
Official's Role
Principal Investigator
Facility Information:
Facility Name
D.O. Ott Research Institute of Obstetrics, Gynecology, and Reproductology
City
Saint Petersburg
ZIP/Postal Code
199034
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
No

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Autologous Bone Marrow-derived Mesenchymal Stem Cells for Atrophic Endometrium in Patients With Repeated IVF Failures

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