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To study the effect of intrauterine Platelet Rich Plasma therapy on pregnancy rates in unexplained infertility

Phase 3
Conditions
Health Condition 1: N979- Female infertility, unspecified
Registration Number
CTRI/2024/01/061002
Lead Sponsor
niversity College of Medical Sciences and Guru Teg Bahadur Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Diagnosed case of Unexplained infertility (documented ovulation, at least unilateral tubal patency, normal uterine cavity and normal semen analysis).

- BMI: 19-25 Kg/m2

Exclusion Criteria

a) Patient on any hormonal therapy or NSAID

b) Female with the diagnosis of hematological disorder and autoimmune disorder.

c) Females with chronic medical disorder such as diabetes, hypertension and tuberculosis.

d) Presence of active infection such Pelvic inflammatory diseases, vaginal or cervical infection

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
a) Comparison of Clinical pregnancy rate with and without PRP therapy in IUI in unexplained infertility. <br/ ><br>b) Comparison of endometrial receptivity with and without PRP therapy in IUI in unexplained infertility.Timepoint: a) 15 days after IUI – UPT will be done <br/ ><br>b) 10-15 days after missed period- TVS for cardiac activity or gestational sac will be done to confirm clinical pregnancy <br/ ><br>c) Endometrial receptivity scoring will be done on the day of IUI, 2 days after IUI, and 4 days after IUI
Secondary Outcome Measures
NameTimeMethod
a) Comparison of luteal phase S. EGF levels with or without PRP therapy in unexplained infertility <br/ ><br>b) Correlation of endometrial receptivity with clinical pregnancy rates <br/ ><br>c) Side effects of PRP therapy in the studyTimepoint: Serum EGF levels after 4 days of IUI
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