Patient-centered Dosage of Levothyroxine

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital of North Norway

About this trial

Levothyroxine is the most used thyroid hormone replacement when the thyroid gland is failing. Because dosage adjustment normally takes several months, the investigators have developed a decision support tool (DST) that predicts optimal dosage based on repeated blood samples the first 2 weeks after initiation of therapy. In this randomized study the investigators will include patients that start levothyroxine therapy after total thyroidectomy. The use of DST to advice the physician about an early dosage adjustment will be compared with common clinical practice, that is dosage adjustment every 2 months. The effect of DST use will be assessed by studying the possible relationship between fast optimal dose adjustment, patient reported outcome measures, and ability to work.

Eligibility criteria

Qualifiers

Total or completion thyroidectomy for differentiated thyroid cancer og benign thyroid nodules at Norwegian hospitals

Disqualifiers

Anaplastic thyroid cancer, thyroid cancer with distant metastasis, graves disease, toxic nodules, pregnancy

Trial design

Treatments tested in this trial

  • Decision support tool

Treatment groups

240 Participants
are divided into 4 treatment groups

Sponsors and collaborators

University Hospital of North Norway

Lead sponsor

SINTEF Health Research

Collaborator

Helseapps

Collaborator

Norinnova

Collaborator

Helse Nord

Collaborator