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Effect of vaginal lactobacillus suppository on in-vitro fertilization (IVF) results

Phase 3
Recruiting
Conditions
Female infertility.
Female infertility of uterine origin
N97.2
Registration Number
IRCT20230718058835N2
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
30
Inclusion Criteria

Age less than 40 years
Maximum FSH level of 15 IU/ml
Absence of any systemic diseases (hypertension, diabetes, antiphospholipid syndrome, lupus, thrombophilia and thyroid diseases)
Normal uterine cavity with sufficient endometrial thickness of 7 mm
Absence of hydrosalpinx

Exclusion Criteria

Diagnosis of Asherman's syndrome
Diagnosis of polyps and fibroids by hysteroscopy
Refusal to participate in the study
Presence of chronic disease
The presence of vaginal infectious discharge
Receiving medical treatment chronically
Repeated IVF failure (more than 3 times in previous cycles)
Presence of clinical symptoms of vaginal infection

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Chemical pregnancy rate. Timepoint: Two weeks after embryo transfer. Method of measurement: Serum level of ß-HCG.
Secondary Outcome Measures
NameTimeMethod
Clinical pregnancy rate. Timepoint: 4-6 weeks after embryo transfer. Method of measurement: Transvaginal ultrasound.
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