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

Phase 2
Conditions
oninflammatory disorder of female genital tract.
Complication associated with artificial fertilization ,unspecified
Registration Number
IRCT20180417039338N2
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
30
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

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

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
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.
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