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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04472234
Other study ID # 2019/15
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2019
Est. completion date September 30, 2019

Study information

Verified date July 2020
Source Sanliurfa Mehmet Akif Inan Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The relationship between BPA elevation in urine, blood, and follicle fluid and embryo quality, IVF/ICSI outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 82
Est. completion date September 30, 2019
Est. primary completion date September 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 23 Years to 33 Years
Eligibility Inclusion Criteria:

- patients aged 23-33 years who underwent IVF due to unexplained infertility

- patients provided urine, blood, and follicle fluid (FF) samples on the oocyte retrieval day

- patients who did not smoke or use alcohol

- patients did not work in the plastic industry

Exclusion Criteria:

- patients who underwent IVF due to low ovarian reserve or tubal factor or male factor indications

- patients diagnosed with endometriosis

- patients with freeze-all cycles

- women with metabolic disease (such as hypertension or diabetes mellitus)

- patients with a known genetic problem (male or female)

Study Design


Intervention

Other:
BPA levels
BPA (Bisfenol A) in urine, blood and follicle fluid samples

Locations

Country Name City State
Turkey Nefise Nazli YENIGUL Sanliurfa

Sponsors (1)

Lead Sponsor Collaborator
Nefise Nazli YENIGUL

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 ürine, blood plasma, and follicular fluid (individual and pooled samples) by use of ELISA test in women with unexplained infertility 6 month
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