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HIPAA Compliant
ISO 27001 Certified

Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
FEMALE
ID06645379

Using Platelet-Rich Plasma PRP to Treat Female Fertility Problems Including Ovarian and Uterine Conditions

Led by The Fourth Affiliated Hospital of Zhejiang University School of Medicine · Updated on 2025-02-18

300

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Female fertility can be affected by several factors including ovarian function, fallopian tube health, the uterine environment, and mental state, with the ovaries and endometrium playing key roles. Common reproductive diseases impacting fertility include ovarian dysfunction, poor ovarian response, intrauterine adhesion, recurrent implantation failure, and thin endometrium. These conditions currently lack effective treatments, and platelet-rich plasma PRP shows promise, prompting further research into its effects and mechanisms. This study evaluates the use of platelet-rich plasma injections delivered via transvaginal or laparoscopic methods for ovarian diseases such as premature ovarian insufficiency and poor ovarian response. For uterine diseases including intrauterine adhesion, thin endometrium, and repeated implantation failure, PRP is administered through intrauterine perfusion or injections under the endometrium. The study focuses on monitoring the safety of PRP treatment up to three months post-enrollment. Participants are female patients aged 18 to 50 years diagnosed with one of the specified reproductive diseases. Their progress will be tracked through assessments of adverse and serious adverse events from enrollment through the three-month treatment period. Researchers will evaluate the safety of PRP injections and collect data to better understand its potential therapeutic effects in reproductive medicine.

CONDITIONS

Brief Title

Application of Platelet-rich Plasma (PRP) in Reproductive Medicine

Who Can Participate

Age: 18Years - 50Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged over 18 and under 40 years with premature ovarian insufficiency characterized by oligomenorrhea or amenorrhea over 4 months and specific hormone or follicle count criteria
  • Women aged up to 50 years with poor ovarian response meeting at least two of three criteria including age, previous IVF response, and ovarian reserve markers
  • Adult women diagnosed with intrauterine adhesion by hysteroscopy, with symptoms and desire to conceive
  • Adult women with thin endometrium defined by thickness less than 7mm on specific cycle days and desire to conceive
  • Women under 40 with repeated implantation failure after at least three embryo transfers of high-quality embryos
Not Eligible

You will not qualify if you...

  • Alanine aminotransferase levels more than three times the normal upper limit or estimated glomerular filtration rate below 90 ml/min
  • Bleeding disorders or use of anticoagulant or antiplatelet drugs
  • Serious mental illness, cardiovascular or cerebrovascular diseases, and malignant tumors
  • Poorly controlled diabetes or other systemic diseases
  • Drug abuse, alcoholism, or drug addiction
  • Participation in other interventional clinical studies within the last six months
  • Poor compliance or any other conditions unsuitable for study participation

Research Team

Y

Youhua Lai

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