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NCT05224284 Clinical Trial

BPA Levels Relationship With IVF/ICSI Outcomes in Patients With Male Factor

IVF Clinical Trial

Official title:
Impact of Blood and Ejaculate Bisphenol A Concentrations on ICSI Cycles Outcome in Patients With Male Factor

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05224284
Other study ID # 2019/21
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2019
Est. completion date October 30, 2019

Study information
Verified date January 2022
Source Sanliurfa Mehmet Akif Inan Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Association between blood and semen BPA levels and ICSI outcomes in patients with male factor

Recruitment information / eligibility
Status Completed
Enrollment 75
Est. completion date October 30, 2019
Est. primary completion date October 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 23 Years to 45 Years
Eligibility Inclusion Criteria: - female patients aged 23-40 years who underwent IVF due to male factor - men with semen sample obtained from ejaculate - male patients provided blood, and ejaculate samples on the oocyte retrieval day - patients who did not smoke or use alcohol - patients did not work in the plastic industry Exclusion Criteria: - men with a diagnosis of azoospermia - patients who underwent IVF due to low ovarian reserve or unexplained infertility indications - patients diagnosed with endometriosis - patients with freeze-all cycles - women with metabolic disease (such as hypertension or diabetes mellitus) - patients (male or females) with a known genetic problem (male or female)

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• BPA levels
BPA (Bisfenol A) in blood and ejaculate samples

Locations
Country Name City State
Turkey Nefise Nazli YENIGUL Bursa

Sponsors (1)
Lead Sponsor Collaborator
Sanliurfa Mehmet Akif Inan Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Exposure to BPA Concentrations of Bisphenol A (BPA) will be quantified in the blood plasma, and ejaculate (individual and pooled samples) by use of ELISA test in women with male factor 6 month
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