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Comparison of sildenafil and estrogen for improvement of uterine health in patients with infertility

Not Applicable
Not yet recruiting
Conditions
Health Condition 1: N972- Female infertility of uterine origin
Registration Number
CTRI/2022/02/040244
Lead Sponsor
SRM College Of Pharmacy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Primary and secondary infertility.

Endometrial lining thickness <7mm in pre-ovulatory phase of menstrual cycle.

Exclusion Criteria

Women with major health problems (i.e.cardiovascular disease,endocrine abnormalities,Renal and liver disease, patients with history of seizures .

Uterine structural anomalies and other pathologies such as endometrial polyps,severe intrauterine adhesion,hydrosalpinx or pyosalpinx.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the improvement in endometrial thickness between vaginal sildenafil and oral <br/ ><br>estradiol valerate in patients with infertility.Timepoint: Baseline ET,5days
Secondary Outcome Measures
NameTimeMethod
To compare the improvement of endometrial vascularity between vaginal sildenafil and <br/ ><br>oral estradiol valerate. <br/ ><br> <br/ ><br>To compare the pregnancy rate outcomes among patients treated with vaginal sildenafil and <br/ ><br>oral estradiol valerate.Timepoint: Baseline PI,5Days <br/ ><br> <br/ ><br>Baseline pregnancy rate ,4weeks
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