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Platelet rich plasma and recurrent implantation failure

Not Applicable
Recruiting
Conditions
recurrent implantation failure.
Female infertility, unspecified
N97.9
Registration Number
IRCT20080831001141N37
Lead Sponsor
ROYAN Institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
40
Inclusion Criteria

Infertile women with a history of recurrent implantation failure
Age 20-40 years
Body Mass Index 19-29 Kg/m2
Having at least three good quality embryos

Exclusion Criteria

Women with hematologic and autoimmune disorders
Couples with chromosomal and genetic abnormalities
Women with uterine anomalies
Women with uterine and ovaries surgical history
Women with endometriosis and adenomyosis
Women with hydrosalpinx
Women with uterine fibroids
Women with recurrent abortion history
Cervicitis
History of fever condition (in up to 2 weeks before the intervention)
Use of corticosteroids (in up to 2 weeks before the intervention) or non-steroid anti-inflammatories (in up to 48 hours before the intervention)
Anemia, thrombocytopenia, platelet dysfunction syndrome, hypofibrinogenemia
Septicemia, active infections with Pseudomonas, Klebsiella or Enterococcus
History of cancer

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ive birth rate; live birth is defined in which a live fetus is delivered beyond 20 completed weeks of gestational. Timepoint: Only once; at least 20 weeks after embryo transfer. Method of measurement: Clinical information.
Secondary Outcome Measures
NameTimeMethod
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