Hysteroscopic Injections of Autologous Endometrial Cells and Platelet-rich Plasma in Patients With Thin Endometrium

Sponsor
Federal State Budget Institution Research Center for Obstetrics, Gynecology and Perinatology Ministry of Healthcare (Other)
Overall Status
Completed
CT.gov ID
NCT05455151
Collaborator
Sechenov University (Other)
115
1
4
29
4

Study Details

Study Description

Brief Summary

The investigation is devoted to the study of the effect of the introduction of autologous platelet-rich plasma (PRP) on the thickness of the endometrium. It was found that the injection of PRP and endometrial cells resuspended in PRP into the endometrium of patients with thin endometrium leads to an increase in the proliferation of endometrial cells, and as a result, to an increase in its thickness.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Conservative therapy
  • Biological: PRP injection
  • Biological: Injection of PRP after conservative therapy
  • Biological: Injection of PRP with endometrial cells
Phase 1

Detailed Description

The study enrolled 115 patients with thin endometrium (<7 mm at implantation window) and infertility. The cohort was divided into groups based on the treatment regimen.

Group 1 (the control, n=30) underwent conservative therapy. Group 2 (n=42) received intraendometrial injections of autologous PRP instead of the conservative therapy. Group 3 (n=38) received identical injections after conservative therapy. Group 4 (n=5) received injections of the minimally manipulated autologous endometrial cells suspended in autologous PRP.

Injections of PRP and endometrial cells suspended in autologous PRP into basal layer of endometrium facilitate the reconstitution by enhancing cell proliferation and angiogenesis.

Study Design

Study Type:
Interventional
Actual Enrollment :
115 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The patients were divided into 4 groups depending on the substances introduced into the basal layer of the endometrium. Group 1 underwent conservative therapy. Group 2 received intraendometrial injections of autologous PRP instead of the conservative therapy. Group 3 received identical injections after conservative therapy. Group 4 received injections of the minimally manipulated autologous endometrial cells suspended in autologous PRP.The patients were divided into 4 groups depending on the substances introduced into the basal layer of the endometrium. Group 1 underwent conservative therapy. Group 2 received intraendometrial injections of autologous PRP instead of the conservative therapy. Group 3 received identical injections after conservative therapy. Group 4 received injections of the minimally manipulated autologous endometrial cells suspended in autologous PRP.
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Hysteroscopic Injections of Autologous Endometrial Cells and Platelet-rich Plasma in Patients With Thin Endometrium - a Pilot Study
Actual Study Start Date :
Oct 1, 2018
Actual Primary Completion Date :
Jan 11, 2021
Actual Study Completion Date :
Mar 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Conservative therapy

This is Group 1, whose patients received electrical impulse therapy using a BTL-4000 Premium G device (BTL Medical Technologies, Czech Republic) starting from day 5-7 of menstrual cycle for 10-12 days daily.

Procedure: Conservative therapy
Conservative therapy to which the patients were subjected was the effect of an electrical impulse

Experimental: PRP injection

This is Group 2, whose patients received single intraendometrial injections of autologous PRP during proliferative phase (day 6-9) of menstrual cycle.

Biological: PRP injection
This intervention consisted of injecting platelet-rich plasma (PRP) into the endometrium

Experimental: Injection of PRP after conservative therapy

This is Group 3, whose patients received electrical impulse therapy identically with Group 1 during the first menstrual cycle. In the second cycle, the patients received autologous PRP injections identically with Group 2.

Biological: Injection of PRP after conservative therapy
This intervention consisted of conducting conservative therapy with an electrical impulse and then injecting PRP inside the endometrium

Experimental: Injection of PRP with endometrial cells

This is Group 4, whose patients received single intraendometrial injections of the minimally manipulated autologous endometrial cells suspended in autologous PRP during proliferative phase (day 6-9) of menstrual cycle.

Biological: Injection of PRP with endometrial cells
This intervention consisted of injecting endometrial cells suspended in prp

Outcome Measures

Primary Outcome Measures

  1. Change in endometrial thickness after treatment compared with control. [Baseline and 2 month]

    Ultrasonography measurements of endometrial thickness before and after the therapy and compare the thickness. Endometrial thickness measured in mm.

  2. The Doppler-assisted detection of the uterine spiral arteries [1 month]

    The number of identified vessels is counted and the percentage of detection frequency is calculated accordingly, adjusted for the McNemar's binomial test. Compare the rates of visualization of the uterine spiral arteries after therapy in all groups of patients.

  3. Study of the effect of therapy on the onset of pregnancy [9 months]

    Investigation of the rates of clinical pregnancies and live births in all groups. After therapy, the number of clinical pregnancy and the number of live births were calculated.

  4. The content of growth factor in autologous PRP [3 month]

    Investigation of the content of platelet-derived growth factor-BB (PDGF-BB) and vascular endothelial growth factor (VEGF) in autologous PRP. Relative levels of PDGF-BB and VEGF are normalized to the total protein content.

  5. Phenotyping of cells isolated from endometrial biopsies [3 month]

    Investigation of cellular composition in endometrial biopsy. The percentage of cells positive for markers of mesenzymal stromal cells, epithelial and endothelial cells, lymphocytes is calculated and the determination of the phenotype of cells in endometrial biopsy.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age 18-40 years

  • Normal karyotype

  • Normal karyotype of the partner

  • Regular ovulatory and menstrual cycle

  • Endometrium <7 mm thick as measured at implantation window

  • Availability of ≥2 vitrified blastocysts of good quality

  • History of implantation failure and/or embryo transfer (ET) cancellation due to insufficient endometrial thickness

Exclusion Criteria:
  • Pathospermia in partner

  • Use of donor gametes

  • Premature ovarian failure

  • Internal genital anomalies

  • Systemic blood diseases and coagulopathy

  • Hemoglobin <100 g/L

  • Platelets <100×109/L

  • Antiplatelet/anticoagulant therapy recipient status

Contacts and Locations

Locations

Site City State Country Postal Code
1 Federal State Budget Institution Research Center for Obstetrics, Gynecology and Perinatology Ministry of Healthcare Moscow Russian Federation 117997

Sponsors and Collaborators

  • Federal State Budget Institution Research Center for Obstetrics, Gynecology and Perinatology Ministry of Healthcare
  • Sechenov University

Investigators

  • Study Director: Inna Apolikhina, MD, FSBI "National Medical Research Center for Obstetrics, Gynecology and Perinatology named after Academician V.I.Kulakov" Ministry of Healthcare of the Russian Federation
  • Principal Investigator: Zulfiia Efendieva, PhD, FSBI "National Medical Research Center for Obstetrics, Gynecology and Perinatology named after Academician V.I.Kulakov" Ministry of Healthcare of the Russian Federation

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Federal State Budget Institution Research Center for Obstetrics, Gynecology and Perinatology Ministry of Healthcare
ClinicalTrials.gov Identifier:
NCT05455151
Other Study ID Numbers:
  • №10-18/11.2018
First Posted:
Jul 13, 2022
Last Update Posted:
Jul 13, 2022
Last Verified:
Jun 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Federal State Budget Institution Research Center for Obstetrics, Gynecology and Perinatology Ministry of Healthcare

Study Results

No Results Posted as of Jul 13, 2022