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Analysis of BPA Concentration in Serum in Women of Reproductive Age With Autoimmune Thyroid Disease

J

Jagiellonian University

Status

Completed

Conditions

Hyperthyroidism
Hypothyroidism
Graves Disease
Hashimoto Disease

Treatments

Diagnostic Test: Serum BPA

Study type

Observational

Funder types

Other

Identifiers

NCT04682340
BPA-Thyroid

Details and patient eligibility

About

The aim of the study is to assess the relationship between the concentration of bisphenol A in serum and selected parameters of thyroid function in women of reproductive age with thyroid dysfunction - Hashimoto's disease and Graves' disease.

Enrollment

80 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Graves' disease or Hashimoto's disease (positive thyroid autoantibody)
  • Control group: thyroid autoantibody negative, normal thyroid function
  • Women aged 18 to 45 in both the control group and experimental group

Exclusion criteria

  • Pregnancy and lactating women
  • Previous or planned treatment with 131I or thyroidectomy
  • The use of drugs affecting the thyroid function (lithium, amiodarone, interferon a, sodium nitroprusside, sunitinib, sorafenib, iodine contrast, antibiotics / antifungals / antivirals (for at least 4 weeks prior to recruitment to the study), which do not result from the treatment of thyroid disease (levothyroxine, thyreostatic drugs, glucocorticoids)
  • Active malignancy
  • Other autoimmune diseases
  • Other endocrine diseases
  • Patients with severe liver, kidney or heart failure

Trial design

80 participants in 3 patient groups

Hashimoto's Group
Description:
Thyroid antibody positive and hypothyroidism
Treatment:
Diagnostic Test: Serum BPA
Graves' Group
Description:
Thyroid antibody positive and hyperthyroidism
Treatment:
Diagnostic Test: Serum BPA
Control Group
Description:
Thyroid antibody negative and euthyroidism
Treatment:
Diagnostic Test: Serum BPA

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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