Efficacy of Thyroid Hormone Replacement for Secondary Hypothyroidism Following Intracerebral Hemorrhage

Intracerebral Hemorrhage Clinical Trial

Official title:

A Study on the Efficacy of Thyroid Hormone Replacement Therapy for Secondary Hypothyroidism Following Intracerebral Hemorrhage

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06353555
• Other study ID #: PUMCH-20240311
• Status: Recruiting
• Phase: N/A
• Start date: October 11, 2023
• Est. completion date: December 31, 2025

Study information

• Verified date: April 2024
• Source: Peking Union Medical College Hospital
• Contact: Junji Wei
• Phone: 15801056698
• Email: weijunji[@]pumch.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Low levels of serum triiodothyronine (T3) thyroid hormones (T4) are a strong predictor of mortality and poor prognosis in critical care patients. Few reports, however, have focused on neurocritical patients.

Patients with severe neurological diseases often experience more complications and exhibit higher mortality rates, and many studies have provided evidence for a low T3/T4 state being an important prognostic indicator in such cases; Lieberman et al. found that 87% of individuals with severe traumatic brain injury have thyroid function below the mid-normal range. Other researchers showed that low T3 syndrome is a predictor of poor prognosis in cerebral infarction patients; their findings indicated the central hypothyroidism and disturbance of thyroid hormone metabolism were involved. Low T3 syndrome is common in patients with brain tumors and has been shown to be associated with shorter survival in glioma patients. Despite these observations, however, whether the thyroid hormone abnormalities in the critically ill are a physiological adaptation or a pathological change, and whether hormone replacement therapy (HRT) can benefit such patients, remain to be established.

As acute progression ceases, thyroid hormone levels may return to normal. This may imply that thyroid hormone supplements could improve the prognosis of patients with secondary hypothyroidism. Previous clinical studies have examined the effect of thyroid HRT on patients undergoing cardiac surgery; patients with malnutrition, heart failure, or acute renal failure; and premature infants with acute respiratory distress syndrome. Most of these past studies found no significant positive effects on prognosis, and no harmful effects either. Some smaller studies have demonstrated potential promise for the use of HRT; for example, one study showed that T3 supplementation in patients undergoing cardiac surgery could lead to less need for inotropic support and better hemodynamic parameters. There are no reports of thyroid HRT improving the prognosis of neurocritical patients with secondary hypothyroidism.

The application of hormone replacement therapy in the treatment of neurocritical patients with secondary hypothyroidism remains controversial.

This study aims to explore the safety and effectiveness of thyroid hormone replacement therapy in patients with spontaneous intracerebral hemorrhage and concomitant secondary hypothyroidism.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: December 31, 2025
• Est. primary completion date: June 1, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Admittance of neurocritical patients to the Neurological Intensive Care Unit (NICU) with a Glasgow Coma Scale (GCS) score of 3-8 and supratentorial hematoma volume >30 ml. The disease is limited to spontaneous intracerebral hemorrhage (supratentorial brain parenchyma, with or without hematoma rupture into the ventricle).

2. Age: 18-80 years old.

3. Onset within 24 hours.

4. Free T3 < 1.80 pg/ml or free T4 < 0.81 ng/dl within 7 days of onset, with or without TSH < 0.38 µIU/ml. (Specifically according to the critical values of different center laboratories' abnormal ranges).

5. Emergency head CT scan completed within 24 hours of onset.

Exclusion Criteria:

1. Organic thyroid lesions (subacute thyroiditis, chronic thyroiditis, post-thyroidectomy, thyroid radiation, hyperthyroidism), history of thyroid hormone oral replacement therapy within the past month.

2. Sella region lesions.

3. Baseline CT indicates irreversible brain herniation, expected survival period <30 days.

4. Severe systemic multiple injuries outside the nervous system.

5. Pregnant women.

6. Acute or chronic heart failure, arrhythmias, myocardial disease.

7. Only TSH levels decrease while free T3 and free T4 levels remain normal.

Related Conditions & MeSH terms

• Cerebral Hemorrhage
• Euthyroid Sick Syndromes
• Hemorrhage
• Hormone Replacement Therapy
• Hypothyroidism
• Intracerebral Hemorrhage
• Low T3 Syndrome

Intervention

Drug:
• Euthyrox
Upon discovering low T3 or low T4 levels, administer oral levothyroxine sodium tablets daily. If accompanied by a decrease in TSH, the regimen is 100µg qd (for individuals weighing <75kg) or 150µg qd (for individuals weighing >75kg). If not accompanied by a decrease in TSH, the regimen is 50µg qd. However, if thyroid function does not significantly improve within 3 days of medication, the regimen is adjusted to 100µg qd. Treatment should continue until transfer out of the NICU or discharge, with a minimum duration of 7 days.
• Euthyrox
Patient will not receive the oral levothyroxine sodium tablets.

Locations

Country	Name	City	State
China	Peking union medical college hospital	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	blood pressure	Systolic blood pressure in mmHg, diastolic blood pressure in mmHg, mean arterial pressure in mmHg, heart rate in beat per minute	Day1?2?3?5?7( 9:00 17:00 21:00)
Primary	cerebral blood flow dynamics	Cerebral blood volume in ml/100g; cerebral blood flow in ml/(100g·min)	Day 7
Primary	Whether to use vasoactive vasopressors	Blood pressure in mmHg before and after using vasoactive vasopressors	Day 1 to 7
Primary	neurological function	modified Ranking Scale score (0 to 6 score, from better to worse)	in 90 days
Secondary	Days of the patients received intensive care		From date of randomization until the date of first documented progression or date of discharge from any cause, whichever came first, assessed up to 12 months
Secondary	Mechanical ventilation time		From date of randomization until the date of first documented progression or date of discharge from any cause, whichever came first, assessed up to 12 months