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OpenTrials
Completed

NCT Number: NCT03249415

Use of PRP in Endometrial Reconstruction

Infertility, which affected 48.5 million couples worldwide in 2010 alone, has many causes; some causes result from issues related to the endometrium. Unfortunately, no cure exists for medical conditions resulting in the destruction of the endometrium, or for non-functional uterus. Thus, safe and effective therapies are needed to treat these diseases and to establish fertility in affected women. These novel techniques refer to the use and application of regenerative/paracrine factors to regenerate the endometrium in patients with Asherman's Syndrome (AS) and Endometrial Atrophy (EA).These new therapies based on the injection of the identified regenerative/paracrine factors and the platelet-rich plasma (PRP) from whole blood in an immunodeficient mouse model with AS/EA, evaluating their contribution and/or effect in the endometrial repair by functional proofs.

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Key information

Age range

25 year–40 year

Sex eligibility

Female

Study type

Observational

Primary location

IVI Barcelona

Barcelona, Spain

About this study

The objective is to know the effect of these regenerative factors obtained from Platelet-Rich Plasma in an immunodeficient murine model with AS/EA Blood from patients with Asherman's Syndrome (AS) and Endometrial Atrophy (EA) will be collected, maintained under anticoagulant solution and after several centrifugations PRP will be obtained. Demonstration of a functional endometrium will be proved determining pregnancy and implantation rates as well as the number of live pups/pregnant female in our mice model. Also, the uterus histology will be analysed in treated and untreated mice

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants diagnosed with Asherman Syndrome and Endometrial Atrophy by Hysteroscopy.
  • No pregnancy after hormonal treatment.

Exclusion criteria

  • Psychiatric diseases.

Treatment and study plan

Primary outcomes

  1. Endometrial thickness after reconstruction in murine model

    Time frame: through study completion, an average of 1 year

    Using histological and functional technologies demonstration of regeneration ability of PRP

Sponsors and collaborators

Lead sponsor

Fundación IVI

Other

Registry information

Official study title

Endometrial Reconstruction by Human Regenerative Factors Derived From Platelet-Rich Plasma in Mice Models

Important dates

Study start
2017
Primary completion
2023
Study completion
2023
First posted
Aug 15, 2017
Registry last updated
Mar 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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