Thyroid Hormone Replacement After Coronary Artery Bypass Grafting for Patients With Subclinical Hypothyroidism

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19-90
SponsorSeoul National University Bundang Hospital

About this trial

The goal of this clinical trial is to find out whether levothyroxine reduces complications and improves the prognosis of patients with subclinical hypothyroidism (SCH) undergoing coronary artery bypass grafting (CABG).

The main questions this study aims to answer are:

• Does levothyroxine reduce major adverse cardiovascular events (MACE), including cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and new arrhythmias, in SCH patients undergoing CABG? Researchers will compare patients who take levothyroxine with those who do not.

Participants will:

* Be randomly assigned to either receive levothyroxine or not * Start the medication one day before surgery if assigned to the treatment group. * Have regular follow-up visits to check thyroid function and cardiovascular events for up to five years after surgery.

Eligibility criteria

Qualifiers

Adults aged 19 to 90 years.

Patients scheduled to undergo coronary artery bypass graft (CABG) surgery.

Subclinical hypothyroidism (SCH), defined as a normal free thyroxine (free T4) level and a thyroid-stimulating hormone (TSH) level greater than 4 μIU/mL, based on testing performed within 31 days prior to surgery.

Disqualifiers

Patients who underwent repeat or emergency CABG surgery

Use of LT4 within the previous 4 weeks

Use of antithyroid drug use (propylthiouracil, methimazole, or carbimazole) within the previous 3 months

Severe comorbid conditions with a life expectancy of less than 1 year (e.g. advanced malignancy)

Trial design

Treatments tested in this trial

  • levothyroxine

Treatment groups

338 Participants
are divided into 2 treatment groups