Assessment of Endometrial and Sub-endometrial Vascularity Before and After PRP Infusion in Frozen Embryo Transfer Cycles
3D Power Doppler Ultrasound Assessment of Endometrial and Sub-endometrial Vascularity Before and After PRP Infusion in Frozen-thawed Embryo Transfer Cycles: a Pilot Study.
1 other identifier
interventional
30
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2020
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 24, 2020
CompletedFirst Posted
Study publicly available on registry
January 29, 2020
CompletedStudy Start
First participant enrolled
February 8, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
October 5, 2020
CompletedJanuary 29, 2020
January 1, 2020
7 months
January 24, 2020
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
EXPERIMENTALInterventions
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.
Eligibility Criteria
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
- Hatem AbuHashimlead
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
- STUDY CHAIR
Hatem Abu Hashim, MD. FRCOG. PhD
Faculty of Medicine, Mansoura University
- PRINCIPAL INVESTIGATOR
Mohamed Taman, MD
Faculty of Medicine, Mansoura University
Central Study Contacts
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