Platelet Rich Plasma for Insufficient Endometrium

Description

To determine the effectiveness of an intrauterine PRP infusion on endometrial thickness and in vitro fertilization (IVF) outcomes in a population of infertile women with a history of unresponsive thin endometrium.

Conditions

Infertility of Uterine Origin

Study Overview

Study Details

Study overview

To determine the effectiveness of an intrauterine PRP infusion on endometrial thickness and in vitro fertilization (IVF) outcomes in a population of infertile women with a history of unresponsive thin endometrium.

Intrauterine Platelet Rich Plasma (PRP) Infusion for Endometrial Insufficiency: A Prospective, Double-Blind, Placebo-Controlled Randomized Controlled Trial

Platelet Rich Plasma for Insufficient Endometrium

Condition
Infertility of Uterine Origin
Intervention / Treatment

-

Contacts and Locations

Basking Ridge

Reproductive Medicine Associates of New Jersey, Basking Ridge, New Jersey, United States, 07920

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Patients who have previously undergone at least 2 unsuccessful frozen embryo transfer cycles, defined as failure to achieve a sustained clinical pregnancy (visualization of intrauterine gestational sac on ultrasound or a cancelled embryo transfer cycle due to inadequate endometrial thickness
  • * Patients with a diagnosis of thin endometrial lining (less than or equal to 6 mm maximum thickness) during prior unsuccessful or canceled embryo transfer cycles.
  • * Fewer than 2 prior unsuccessful or canceled frozen embryo transfer cycles.
  • * Most recent unsuccessful embryo transfer prior to January 1, 2017.
  • * Mullerian anomalies, excluding arcuate uterus
  • * Concurrent submucosal fibroids, unrepaired uterine defects or present indication for uterine surgery
  • * Communicating hydrosalpinx without plans for surgical correction prior to study enrollment.
  • * Failure of patient to agree to enrollment in study with written consent.
  • * Concurrent pregnancy
  • * Anticoagulation use for which plasma infusion is contraindicated
  • * History of thrombosis
  • * Thrombophilia either inherited or acquired
  • * Concomitant use of adjunctive therapies for proliferation. These must be discontinued upon enrollment.
  • * Embryo planned to be used for transfer generated from surgically obtained sperm due to a diagnosis of non-obstructive azoospermia
  • * Recurrent/persistent endometrial fluid in prior cycles

Ages Eligible for Study

18 Years to 45 Years

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Reproductive Medicine Associates of New Jersey,

Study Record Dates

2025-12