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Improvement of laboratory diagnostics in hypothyroid patients using levothyroxine.

Improvement of laboratory diagnostics in hypothyroid patients using levothyroxine. - ANTICIPATE

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON53877
Enrollment
600
Registered
2022-05-19
Start date
2022-07-26
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hypothyroidism slow acting thyroid slow acting thyroid

Interventions

None listed

Sponsors

Amsterdam UMC
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Hypothyroid patients - Ability to provide informed consent; - Ability to speak and understand Dutch or English - Intake of a stable dose of levothyroxine, meaning the dosage of levothyroxine must not be changed during the appointment at the outpatient clinic - Diagnosis of one of these forms of hypothyroidism O Patients with primary hypothyroidism: euthyroid based on TSH according to physician O Patients with hypothyroidism after a total thyroidectomy due to thyroid carcinoma (therefore athyroid): on target TSH according to physician (target TSH depending on stage/severity of carcinoma) O Patients using L-T4 due to therapy of Graves* disease: euthyroid based on TSH according to physician (TSH cannot be suppressed, namely TSH within reference interval of 0,5-5,0 mU/L) O Patients with central hypothyroidism: euthyroid based on fT4 according to physician (common is fT4 in the upper limit, reference interval is 12-22 pmol/L) Healthy controls - Ability to provide informed consent; - Ability to speak and understand Dutch or English - Consider themselves healthy

Exclusion criteria

Exclusion criteria: Hypothyroid patients - Not euthyroid according to physician - Pregnant - Patients using L-T4 due to the treatment of Graves* disease: if TSH is still suppressed - Any of the following medication o Iodide o Liothyronine (Cytomel) o Oral anticonceptiva o Active treatment of malignancy (except DTC) Healthy controls - Pregnancy - Any of the following medication o Thyroid medication (a.o. levothyroxine, thiamazol, PTU) o Lithium o Amiodarone o Propranolol o Iodide o Glucocorticoids o Oral contraceptives o Heparin o Growth hormone o Active treatment of malignancy

Design outcomes

Primary

MeasureTime frame
fT3, fT3/fT4 ratio and fT4 and TSH concentrations.

Secondary

MeasureTime frame
- Laboratory tests: rT3, TT4, TT3, SHBG, acylcarnitine profile, tyrosine, phenylalanine, serine and DIO1/2/3 polymorphisms - Questionnaire: ThyPRO-39

Countries

Netherlands

Contacts

Public ContactK.M. Latupeirissa

Amsterdam UMC

k.m.latupeirissa@amsterdamumc.nl0612543142

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Feb 3, 2026