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OpenTrials
Completed

NCT Number: NCT03166345

Use of Platelet Rich Plasma (PRP) for Improving Thin Endometrium

Platelets rich plasma is simple source of growth factors and cytokines that can regulate endometrial growth for subgroup of thin endometrium women. It is an autologous source of this enhancing factors; therefore, there os no risk of using it within the same participant.

Completed

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Key information

Conditions

Poor Endometrium

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Gannah IVF unit, Gannah Hospital, Giza, Egypt

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • women with thin endometrium

Exclusion criteria

  • serum positive hepatitis B and C women

Treatment and study plan

Treatment of Thin Endometrium

Other

This is a trial to improve endometrial thickness by autologous injection of PRP into the Uterine Cavity compared with CSF or no treatment.

Primary outcomes

  1. Mean Diameter of endometrial thickness

    Time frame: 2 days

    How the endometrium would respond after 2 days of PRP

Secondary outcomes

  1. Clinical pregnancy rate

    Time frame: 4 weeks or beyond after embryo Transfer

    Registered fetal heartbeat 4 weeks or beyond after embryo transfer.

Sponsors and collaborators

Lead sponsor

Ibn Sina Hospital

Other Gov

Collaborators

  • Ganna Hospital

Registry information

Official study title

Use of Platelet Rich Plasma (PRP) for Improving Thin Endometrium For IVF Women

Acronym: PRPITM

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
May 25, 2017
Registry last updated
Jul 12, 2018

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.