Autologous Platelet Rich Plasma (PRP) Intra Ovarian Infusion in Perimenopausal Women
Recruiting now · Phase 2/Phase 3 · Has a placebo group
Conditions studied: Infertility, Female, Perimenopausal Disorder, Menstrual Cycle Abnormal
In brief
Autologous PRP intra ovarian infusion may improve ovarian response and women's hormonal profile and may promote folliculogenesis in perimenopausal women.
Key facts
- Study ID
- NCT03951194
- Run by
- Genesis Athens Clinic
- People needed
- 100
- Starts
- 2019-06-13
- Expected to finish
- 2028-07-30
- Last updated by the study team
- 2026-07-08
Who can join
Age: 40 and older, up to 50. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Women ≥40 years of age, presenting with cycle irregularities while fulfilling at least one of the respective two criteria: more than seven days difference in menstrual cycle duration between two consecutive cycles OR, presence of a menstrual cycle duration over sixty days and progressive elevation of FSH levels.
- Discontinuation of any complementary/adjuvant treatment including hormone replacement, acupuncture, and botanotherapy, for at least three months prior to recruitment.
- Willing to comply with study requirements
You may not qualify if…
- Any pathological disorder related to reproductive system anatomy
- Amenorrhea
- Endometriosis
- Adenomyosis
- Fibroids and adhesions
- Infections in reproductive system
- Current or previous diagnosis of cancer in reproductive system
- History of familiar cancer in reproductive system
- Severe male factor infertility
- Prior referral for PGT
- Ovarian inaccessibility
- Previous POI diagnosis -Endocrinological disorders (Hypothalamus-
- Pituitary disorders, thyroid dysfunction, diabetes mellitus, metabolic syndrome)
- BMI>30 kg/m2 or BMI<18.5 kg/m2
- Systematic autoimmune disorders
Where it is running
- Genesis AC — Athens, Greece (enrolling)
Full record on ClinicalTrials.gov
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