CClinicalTrials.gg
Status unknownNCT02973555Updated Nov 25, 2016

Platelet-Rich Protein and the Endometrium

An interventional study of PRP injection in Infertility, sponsored by Hadassah Medical Organization. Status unknown at 1 site in Israel. Open to female participants aged 18 Years to 54 Years. Per ClinicalTrials.gov, last updated 2016-11-25.

Sponsored by Hadassah Medical Organization · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Nov 2016), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Not applicable
Ages
18 Years to 54 Years
Sex
Female
01

Study summary

Platelet-rich plasma (PRP) may promote the endometrial growth and improve pregnancy outcome of patients with thin endometrium undergoing ART treatments.

02

Conditions studied

  • Infertility

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03

In context

Infertility

2,506 studies on the registry are indexed under Infertility; 407 are open to participants now.

This study's planned enrollment of 50 is below the median of 120 across 1,698 interventional studies indexed under Infertility.

Browse Infertility studies →

Lead sponsor

Hadassah Medical Organization is the lead sponsor of 659 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 54 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Women undergoing a frozen thawed embryo transfer cycle with poor endometrial response to estrogen (\< 7 mm) after at least two standard preparation protocols, of which one was canceled due to thin endometrium

Exclusion criteria

Exclusion Criteria:

  • none
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    PRP injection

    Other: PRP injection

Interventions

  • OtherPRP injection

    autologous intrauterine infusion of PRP

06

What researchers measure

Primary outcomes

  1. endometrial thickness >7mm

    Time frame: 1 month

Secondary outcomes

  1. Positive serum pregnancy test

    Time frame: 14 days post embryo transfer

07

Study locations

1 site
  • Hadassah Medical Organization
    Jerusalem, Israel
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 25, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02973555
Lead sponsor
Hadassah Medical Organization
Responsible party
Sponsor
First posted
Nov 25, 2016
Start date
Jan 2017
Primary completion
Jan 2018 (estimated)
Completion
Jan 2019 (estimated)
Last update
Nov 25, 2016

Study contacts

Ronit Kochman, MD
Contact
kochman@hadassah.org.il
+972 508946414
Ronit Kochman, MD
principal investigator · Hadassah Medical Organization

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2016. You cannot join it, but the record below documents what was studied.

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