NCT04247204

Brief Summary

A good quality embryo and receptive endometrium are important aspects in achieving optimal outcomes in assisted reproductive treatment (ART). Endometrial thickness is an important marker of uterine receptivity. A thin endometrium defined by an endometrial thickness ≤7mm was reported as a poor factor associated with significantly lower implantation and pregnancy rates as well as a higher risk of miscarriage. Nowadays, platelet-rich plasma (PRP) intrauterine infusion is a promising approach for the treatment of refractory thin endometrium in patients undergoing frozen-thawed embryo transfer. This is based on its ability to stimulate proliferation and angiogenesis with a large number of growth factors and cytokines i.e. the endometrium becomes thicker, with higher vascularity. PRP is easily prepared from an autologous blood sample that eliminates the risk of immunological reactions and transmission infections at low cost. Endometrial blood flow is another important marker reflective of uterine receptivity. Although publications are increasing concerning the efficacy of PRP intrauterine infusion on endometrial expansion and proliferation in frozen-thawed embryo transfer cycles, yet its angiogenetic effects have not been evaluated so far in either thin endometrium or normal endometrium thickness. Our study aims to evaluate endometrial and sub-endometrial vasculature patterns before and after PRP infusion in frozen-thawed embryo transfer cycles with normal endometrium thickness.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2020

Shorter than P25 for not_applicable

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 24, 2020

Completed
5 days until next milestone

First Posted

Study publicly available on registry

January 29, 2020

Completed
10 days until next milestone

Study Start

First participant enrolled

February 8, 2020

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2020

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 5, 2020

Completed
Last Updated

January 29, 2020

Status Verified

January 1, 2020

Enrollment Period

7 months

First QC Date

January 24, 2020

Last Update Submit

January 28, 2020

Conditions

Outcome Measures

Primary Outcomes (1)

  • Vascularization index of the endometrial region

    Vascularization index of the endometrial region will be measured by a researcher using the built-in VOCAL (Virtual Organ Computer-Aided Analysis) software for 3D power Doppler analysis.

    Day 15 to 18 of the frozen embryo transfer cycle

Secondary Outcomes (5)

  • Flow index of the endometrial region

    Day 15 to 18 of the frozen embryo transfer cycle

  • Vascularization flow index of the endometrial region

    Day 15 to 18 of the frozen embryo transfer cycle

  • Vascularization index of the sub-endometrial region

    Day 15 to 18 of the frozen embryo transfer cycle

  • Flow index of the sub-endometrial region

    Day 15 to 18 of the frozen embryo transfer cycle

  • Vascularization flow index of the sub-endometrial region

    Day 15 to 18 of the frozen embryo transfer cycle

Study Arms (1)

Platelet-rich plasma (PRP) intrauterine infusion

EXPERIMENTAL
Biological: Platelet-rich plasma intrauterine infusion

Interventions

For all women, basic transvaginal sonography will be done in the 2nd day of frozen embryo transfer (FET) cycle and they will receive standard hormone replacement therapy (HRT) in the form of estradiol valerate tablets (white tablets of Cyclo-Progynova; Bayer Schering Pharma AG, Germany) at a dose of 4mg for 7 days then 6mg for 6 days. Endometrial assessment will be done on day 15 of FET cycle. Those with endometrial thickness between 8-14 mm will be evaluated for endometrial and sub-endometrial vasculature pattern by 3D power Doppler analysis. Then 1 ml of PRP (prepared from autologous blood) will be infused in the uterine cavity and vaginal progesterone 400 mg twice daily will be prescribed for 3 days. Subsequently, D3 embryos will be transferred. Endometrial, sub-endometrial and uterine arterial vascularity pattern will be re-evaluated on the day of ET. Both estradiol valerate tablets and vaginal progesterone will be continued up to 12th week of gestation in case of pregnancy.

Platelet-rich plasma (PRP) intrauterine infusion

Eligibility Criteria

Age20 Years - 35 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Subfertile women undergoing frozen-thawed embryo transfer with at least previously failed one ICSI cycle.
  • Age between 20-35 years.
  • Women with endometrium thickness between 8-14 mm on D15 of the frozen embryo transfer cycle

You may not qualify if:

  • Women with a thin endometrium (≤ 7 mm) on day 15 of the cycle.
  • Women with known hematological or immunological disorders
  • Women with uncontrolled endocrine or other medical conditions, such as hyperprolactinemia or thyroid diseases.
  • Women with uterine abnormalities e.g. Asherman syndrome, myomas, uterine septum, bicornuate uterus.
  • Women who refuse to participate in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (1)

  • Nandi A, Martins WP, Jayaprakasan K, Clewes JS, Campbell BK, Raine-Fenning NJ. Assessment of endometrial and subendometrial blood flow in women undergoing frozen embryo transfer cycles. Reprod Biomed Online. 2014 Mar;28(3):343-51. doi: 10.1016/j.rbmo.2013.11.004. Epub 2013 Nov 22.

    PMID: 24447958BACKGROUND

Study Officials

  • Hatem Abu Hashim, MD. FRCOG. PhD

    Faculty of Medicine, Mansoura University

    STUDY CHAIR
  • Mohamed Taman, MD

    Faculty of Medicine, Mansoura University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Hatem Abu Hashim, MD. FRCOG.PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

January 24, 2020

First Posted

January 29, 2020

Study Start

February 8, 2020

Primary Completion

August 31, 2020

Study Completion

October 5, 2020

Last Updated

January 29, 2020

Record last verified: 2020-01