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effect of platelet-rich plasma(PRP)on fertility in women

Effect of platelet-rich plasma on clinical pregnancy outcome of women with recurrent implantation failure undergoing ART

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180417039338N2
Enrollment
30
Registered
2018-06-18
Start date
2017-03-21
Completion date
Unknown
Last updated
2018-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Noninflammatory disorder of female genital tract. Complication associated with artificial fertilization ,unspecified

Interventions

Intervention 1: Control group: Continue estradiol since day 2 of cycle till end of study. Intervention 2: Intervention group: Infusion of 0.5 cc of platelet rich plasma( PRP)that contained platelet 4

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Healthy women between 18 and 40 years old BMI below 30 kg / m 2 Have at least 3 or more unsuccessful fetal transmissions Fetal removal candidate

Exclusion criteria

Exclusion criteria: Hemoglobin disorders (hemoglobin less than 11 mg / ml and platelet below 150,000) Immunological disorders Hormonal disorders of genetic and chromosomal anomalies Acute infection Uterus anomalies including the unicorn uterus (whether or not surgical) arcuate History of uterine enzymes such as myomectomy and cesarean section NSAID use within 10 days before intervention Corticosteroid use over the past 1 month Smoking Fever History of malignancy Coagulation disorder

Design outcomes

Primary

MeasureTime frame
Fetal Vision Imaging. Timepoint: Week 5 after ET. Method of measurement: Vaginal ultrasound.;Fetal heartburn. Timepoint: Week 5 after ET. Method of measurement: Vaginal ultrasound.;Endometrial thickness. Timepoint: in 10th day of cycles and 72 hr after infusion of PRP. Method of measurement: Trans vaginal sonography.

Secondary

MeasureTime frame
Determine the amount of implantation. Timepoint: 4week after embryo transfer. Method of measurement: Trans vaginal sonography.;Clinical pregnancy or miscarriage. Timepoint: 4week after embryo transfer. Method of measurement: Trans vaginal sonography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Fatemeh Aghajanzadeh

Babol University of Medical Sciences

aghanjanzadeh@yahoo.com+98 11 3223 8284

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026