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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04019509
Other study ID # TgABstudy Brussels
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2019
Est. completion date September 1, 2022

Study information

Verified date July 2019
Source Universitair Ziekenhuis Brussel
Contact valerie uvin, md
Phone 486073292
Email valerieuvin@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The influence of thyroid autoantibodies on thyroid function in pregnancy after fertility treatment is not well known.

The objectives of the present study are:

1. To monitor the course of thyroid function during pregnancy and to compare between women with and without thyroid autoantibodies.

2. Compare pregnancy outcome between women with and without thyroid antibodies


Description:

Thyroid autoantibodies and / or abnormal thyroid function are associated with fertility problems.

A possible explanation for this is, an influence of thyroid autoantibodies on the functioning of the thyroid gland. It is therefore recommended to check thyroid gland function and for the presence of autoantibodies before pregnancy. In general, 2 types of thyroid autoantibodies are known: anti-thyreoperoxidase autoantibodies and anti-thyroglobulin autoantibodies.

In case of abnormal thyroid function, treatment is sometimes necessary in regards to fertility. The risk of abnormal thyroid function is increased in women with thyroid autoantibodies during pregnancy. Therefore, thyroid function is regularly monitored during pregnancy in women with thyroid antibodies. The influence of thyroid autoantibodies on thyroid function in pregnancy after fertility treatment is not well known.

The objectives of the present study are:

1. To monitor the course of thyroid function during pregnancy and to compare between women with and without thyroid autoantibodies.

2. Compare pregnancy outcome between women with and without thyroid antibodies


Recruitment information / eligibility

Status Recruiting
Enrollment 900
Est. completion date September 1, 2022
Est. primary completion date January 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 36 Years
Eligibility Inclusion Criteria:

- first cycle of assisted reproductive technology with follow up of thyroid function at the Universitair Ziekenhuis Brussel

- age >= 18 and <= 36 years

- body mass index between 18 and 35

Exclusion Criteria:

- Patients with clinical thyroid dysfunction

- Patients being treated with levothyroxine or antithyroid drugs

- Patients being treated with glucocorticosteroids

- Patients undergoing in vitro maturation or preimplantation genetic testing.

- Poor responders during IVF/ICSI stimulation, using the Bologna criteria

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
blood test
blood test for thyroid antibodies and thyroid function (TSH, FT4)
Other:
follow up treatment outcome
questionnaire for treatment outcome: pregnancy, no pregnancy, miscarriage, delivery

Locations

Country Name City State
Belgium UZ Brussel Brussels

Sponsors (1)

Lead Sponsor Collaborator
Universitair Ziekenhuis Brussel

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary thyroid fonction TSH, FT4 evolution during pregnancy 12 months
Primary cumulative delivery rate live birth delivery after IVF stimulation 12 months
Secondary cumulative pregnancy rate pregnancy rate after IVF stimulation 12 months
Secondary miscarriage rate miscarriage rate after IVF stimulation 12 months
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