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Thyroid Gland DiseaseAnti-TPONCT04249271

Antithyroidal Antibodies With or Without Subclinical Hypothyroidism During Pregnancy in Infertile Women

An observational study of Thyroid Gland Disease and Pregnancy Complications, run by University Hospital, Basel, Switzerland at 1 site in Switzerland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

One prospective observational study was carried out in 2009 aiming at identifying the fluctuations of the thyroid hormones in women with normal thyroid gland and in women with anti-TPO antibodies. Serum samples were collected periodically during and after pregnancy in previously infertile women. Read more about this study

Who is it for?
Ages 18 to 40 years, women onlyHealthy volunteers can take part
What is being tested?
serum sampling
How many people
96 participants
Where
1 siteSwitzerland
Study dates
1 Feb 2018to 31 Dec 2019
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Study population: Healthy women having become pregnancy after infertility.

Who may be able to join

  • previous infertility with known thyroidal function (TSH, anti-TPO)

Who cannot join

  • other endocrine pathology, such as Addison, diabetes mellitus
  • manifest thyroidal pathology, such as Graves disease
  • contraindication against pregnancy
  • after repeated miscarriage (3 or more)
  • heavy smokers (20 cig per day or more)

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • Klinik für Gyn. Endokrinologie und Reproduktionsmedizin der Frauenklinik des Universitätsspitals

    Basel, 4031

Other trials in Switzerland

About this study

Official title: Antithyroidale Antikörper Mit Oder Ohne Subklinische Hypothyreose Bei Weiblicher Infertilität in Der Schwangerschaft Und im Wochenbett.

One prospective observational study was carried out in 2009 aiming at identifying the fluctuations of the thyroid hormones in women with normal thyroid gland and in women with anti-TPO antibodies. Serum samples were collected periodically during and after pregnancy in previously infertile women. The samples were stored frozen at -80 °C. Now, the hormone measurements will be carried out.

Read the detailed description

Exclusion of thyroid disease has long been an integral part of a comprehensive infertility work-up, because thyroid function disorders are also associated with disturbances in the menstrual cycle and can cause complications during pregnancy. Subclinical hypothyroidism is the most frequent disease of the thyroid in women of reproductive age (affecting 5 to 10 %). For a long time, measurement of TSH concentration was the only screening parameter used to exclude thyroid disorders. Not only has the differentiation of normal thyroid function (euthyroidism) from the pathological range been controversial for some years but, recently, the role of an elevated anti-TPO antibody titre has also been identified as a significant and independent risk factor for miscarriages and for complications during late pregnancy, even in otherwise euthyroid women. This discovery implies that solely determining the TSH concentration is insufficient. The mechanism underlying the increased rate of complications during pregnancy is also unclear.

The investigators therefore performed a double study to clarify the relative importance of the various possible parameters of thyroid function in the context of an infertility work-up:

  1. Prevalence study: Measurement of TSH and anti-TPO concentrations in 175 women who present with infertility at the Infertility Clinic at the Women's Hospital, University Hospital Basel. In addition, each participant underwent an ultrasound scan of the thyroid. Control group: 175 healthy women of reproductive age and with regular menstrual cycles, but not currently wishing to have children (recruited via posters in the university and Blood Donor Centre). This study has been finished in 2010. The data of the prevalence study were used to carry out the prospective sampling of the serum samples.
  2. Prospective measurement of fluctuations in thyroid function during pregnancy and post-partum in a group of euthyroid women and/or those with subclinical hypothyroidism (TSH > 4.5 mIU/l) with/without anti-TPO antibodies. Two different euthyroid groups were defined for the study: Euthyroidism I = TSH 0.3-2.5 mIU/l; Euthyroidism II = TSH 2.5-4.5 mIU/l. Six groups, each with 16 women, divided according to TSH concentration and anti-TPO antibody status, will be required (total 96). All female participants with subclinical hypothyroidism (TSH concentration > 4.5 mIU/l, normal values of peripheral thyroid hormones) receive a T4 supplementation dose. Serum samples will be collected each week from the start of pregnancy up to the 12th week and stored frozen at -80 °C. Thereafter, a serum sample will be collected once a month (up to the 38th week) and stored frozen at -80 °C. Finally, one serum sample post-partum (4 to 6 weeks after delivery) and freeze it. A total of 96 women (16 in each group) were recruited to participate in this study.

After conclusion of the observation period, levels of the following hormones will be measured in the total of 1120 serum samples: TSH, total and free l-thyroxine and fT4 index, total and free triiodothyronine, thyroid autoantibodies (TPO antibodies), hCG, 17β-oestradiol, progesterone, prolactin.

Being tested
serum sampling
Keywords
thyroid, antibody, pregnancy, infertility
Medical subject headings
Thyroid Diseases, Pregnancy Complications, Infertility

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • serum samplingOther

    repeated serum sampling during pregnancy and thereafter

Study groups in NCT04249271
Study groupRoleWhat they receive
euthyroid, no antibodiesTSH 0.3 to 2.5 mIU/l and anti-TPO <100 IU/ml repeated serum sampling
Receives: Other: serum sampling
borderline euthyroid, no antibodiesTSH 2.5 to 4.5 mIU/l and anti-TPO <100 IU/l repeated serum sampling
Receives: Other: serum sampling
hypothyroidism, no antibodiesTSH >4.5 mIU/l and anti-TPO <100 IU/ml repeated serum sampling
Receives: Other: serum sampling
euthyroid, with antibodiesTSH 0.3 to 2.5 mIU/l and anti-TPO >100 IU/ml repeated serum sampling
Receives: Other: serum sampling
borderline euthyroid, with antibodiesTSH 2.5 to 4.5 mIU/l and anti-TPO >100 IU/l repeated serum sampling
Receives: Other: serum sampling
hypothyroidism, with antibodiesalTSH >4.5 mIU/l and anti-TPO >100 IU/ml repeated serum sampling
Receives: Other: serum sampling

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Deviations from euthyroid function as given by serum levels of TSH (expressed in mIU/l) during pregnancy and after birth.

    Impact of antibodies on thyroid function during pregnancy.

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Jan 2020
  2. Study start1 Feb 2018
  3. Primary completion31 Dec 2019
  4. Study completion31 Dec 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
96 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04249271
Sponsor's protocol ID
EKNZ 39-009 00960
Acronym
Anti-TPO
Status last verified
Jan 2020
First submitted
17 Feb 2018
Last updated
30 Jan 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The serum samples are coded and cannot be traced back to individual patients.

Questions about this trial

What is this clinical trial studying?

An observational study of Thyroid Gland Disease and Pregnancy Complications, run by University Hospital, Basel, Switzerland at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 30 Jan 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Deviations from euthyroid function as given by serum levels of TSH (expressed in mIU/l) during pregnancy and after birth. (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Jan 2020.

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