Status:

COMPLETED

Study of PRP in Women With Evidence of Diminished Ovarian Reserve

Lead Sponsor:

Center for Human Reproduction

Conditions:

Diminished Ovarian Reserve

Ovarian Failure

Eligibility:

FEMALE

21-52 years

Phase:

NA

Brief Summary

The hypothesis of the study is that ovaries of women with a history of poor response to ovulation induction may benefit from exposure to growth factors known to be present in Platelet Rich Plasma (PRP...

Detailed Description

The hypothesis of the study is that ovaries of women with a history of poor response to ovulation induction may benefit from exposure to growth factors known to be present in PRP. Autologous Platelet...

Eligibility Criteria

Inclusion

  • Women with failure to respond well to ovulation induction by having fewer than 1 cleavage stage embryo in response to past ovulation induction who do not qualify for the PRP4POI study
  • Age 54 years and under.
  • FSH \> 12
  • AMH \< 1.1
  • -No Aspirin or Motrin for one week before treatment

Exclusion

  • Age \> 54 years
  • Marked thrombocytopenia
  • Blood diseases
  • Hypofibrinogenemia
  • Hemodynamic instability
  • Anticoagulant or antiaggregant treatment
  • Oncological diseases (specially, skeletal system and blood)
  • Sepsis
  • Acute and chronic infectious diseases
  • Autoimmune diseases, for example, lupus erythematosus, etc.
  • Relative contraindications for PRP
  • Chronic liver diseases in the exacerbation phase
  • Chronic intoxication against the background of long-term use of alcohol, addictive drugs, an administration of potent medications
  • Use of steroidal anti-inflammatory drugs in less than 2 days before drawing the blood, an injection of corticosteroids in little less than 2 weeks before the procedure
  • Pregnancy
  • Inflammatory skin diseases, chronic dermatosis in the exacerbation phase, for example, psoriasis, atopic eczema, etc.

Key Trial Info

Start Date :

October 1 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 1 2024

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT04275700

Start Date

October 1 2018

End Date

September 1 2024

Last Update

May 7 2025

Active Locations (1)

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1

Center For Human Reproduction

New York, New York, United States, 10021