Genesis AC
Athens, 15232, Greece
Location status: Recruiting
NCT Number: NCT03951194
Autologous PRP intra ovarian infusion may improve ovarian response and women's hormonal profile and may promote folliculogenesis in perimenopausal women.
Interested in participating?
Request Info40 year–50 year
Female
Interventional
Phase 2 / Phase 3
Athens, 15232, Greece
Location status: Recruiting
This triple-blind Randomized Controlled Trial (RCT) aims to investigate the effectiveness of autologous PRP intra ovarian infusion on improving ovarian tissue functionality and hormonal profile of perimenopausal women. PRP is blood plasma prepared from fresh whole blood that has been enriched with platelets. It is collected from peripheral veins and contains several growth factors such as vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), platelet derived growth factor (PDGF), transforming growth factor (TGF) and other cytokines all of which stimulate tissue proliferation and growth. PRP has been employed in several medical conditions in Orthopedics, Dermatology, and Ophthalmology for wound healing. It's efficacy in ovarian rejuvenation and reactivation and endometrial regeneration has not been fully elucidated. This study aims to investigate the effect of autologous PRP intra ovarian infusion on improving ovarian tissue functionality in perimenopausal women.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Autologous PRP intra ovarian infusion
Other names: PRP, Platelet Rich Plasma
Autologous PFP intra ovarian infusion
Other names: PFP, Platelet Free Plasma
Time frame: Three months
Regular Menstrual cycle
Time frame: Follow-up period of three months entailing monthly evaluation
Serum FSH levels evaluated monthly for three consecutive months.
Time frame: Follow-up period of three months entailing monthly evaluation
Serum AMH levels evaluated monthly for three consecutive months.
Time frame: Follow-up period of three months entailing monthly evaluation
Serum LH levels evaluated monthly for three consecutive months.
Time frame: Follow-up period of three months entailing monthly evaluation
Serum etsradiol levels evaluated monthly for three consecutive months.
Time frame: Follow-up period of three months entailing monthly evaluation
Serum progesterone levels evaluated monthly for three consecutive months.
Time frame: Follow-up period of three months entailing monthly evaluation
AFC evaluated monthly, on day 2 of the menstrual cycle, for three consecutive months.
Contact information is provided by the study sponsor or research team.
Agni Pantou, MD, PhD Candidate
CONTACT
Mara Simopoulou, PhD
CONTACT
Genesis Athens Clinic
Other
Investigating Improvement of Ovarian Function Following Autologous PRP Intra-ovarian Infusion in Perimenopausal Women
Acronym: PRP
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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