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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04613323
Other study ID # Priamar001
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date September 1, 2022

Study information

Verified date November 2020
Source Centro Diagnostico Priamar
Contact Massimo Giusti, MD
Phone 39 3391753444
Email omsv1416@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The management of thyroid function in pregnancy has been object of several guidelines in the last years. Normal thyroid function reduces prenatal and post-natal risks and gestational complaints. Trimester specific reference values of thyroid hormones and thyroid stimulating hormone (TSH) are available for selected geographic population but its are not yet are available in our country. Hashimoto's thyroiditis (HT) is the most frequent autoimmune thyroid disease which can induce thyroid dysfunction, mainly sub-clinical hypothyroidism. Due to the large incidence in women HT and its potential link with thyroid dysfunction this disease could be search and monitored before pregnancy. Anyway a strong recommendation is to test TSH levels in all patients seeking pregnancy at risk for thyroid dysfunction for a history or current symptoms/signs of thyroid dysfunction, known positivity od thyroid autoimmunity or goiter, a history of neck radiation, age >30 years, diabetes mellitus, previous infertility or pregnant loss, morbid obesity, living in area of moderate-severe iodine deficiency or recent administration of drugs/substance interfering with thyroid function.


Description:

The aim of the study was to retrospectively evaluate from 2011 (data of publication of the first American Thyroid Association (ATA) guidelines for thyroid dysfunction in pregnancy) to now medical record of the a secondary level endocrine unit to verify the adherence to guidelines in the management of thyroid function in pregnant women with HT. The investigators search 1. the adherence to clinical and biochemical endocrine evaluations before conception 2. the use (correct/un-correct) of L-T4 intervention and its monitoring 3. the difference in thyroid function control between women with a fix increment of- L-T4 posology (25 mcg/week more for each 2 kg increment in body weight) after the initial L-T4 adjustment or prescription 4. the clinical and biochemical endocrine evaluation 1-2 months after delivery 5. the outcome of pregnancy 6. the e-mail up-to-date survey on current of off-springs health


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date September 1, 2022
Est. primary completion date July 1, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: Adult HT pregnant women and adult pregnant women with nodular goiter with or whiteout previous known hypothyroidism. Exclusion Criteria: 1. significant pre-pregnancy comorbidity including renal failure, severe liver disease, organ transplant, cardiac failure, psychiatric conditions requiring in-patient admission, history of eating disorder. 2. unable to have e-mail address 3. unavailable written consent 4. unable understand Italian language

Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Centro Diagnostico Priamar

Outcome

Type Measure Description Time frame Safety issue
Primary Control of thyroid function in pregnancy Thyroid hormones and TSH Through study completion, an average of 1 year
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