Thyroid Hormone Replacement for Subclinical Hypothyroidism (TRUST)

NHS Trust

Status and phase

Completed

Phase 4

Conditions

Subclinical Hypothyroidism

Treatments

Drug: Levothyroxine

Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT01660126

2011-004554-26 (EudraCT Number)

GN11GE272

Details and patient eligibility

About

Subclinical hypothyroidism (SCH) is a common condition among older men and women. Although by definition SCH comprises biochemically mild thyroid hormone deficiency without overt symptoms, it is a possible contributor to multiple problems in older age. Thyroid hormone has effects on numerous physiological systems, including the vascular tree, heart, skeletal muscle and brain. Therefore, thyroxine substitution to overcome thyroid hormone deficiency has the potential to give multisystem benefits to older people with SCH.

Small studies have reported reduced atherosclerosis and improved heart function with thyroxine replacement, but no large clinical trials have been performed. Therefore the available evidence is limited, leading to major variations in guidelines and clinical practice, with uncertainty regarding the indications for screening and treatment. The investigators propose a multicentre randomised placebo controlled trial to assess the impact of thyroxine replacement in a minimum of 540 older adults (maximum 750) with persisting SCH (excluding those in whom it is a temporary phenomenon who are unlikely to benefit). The investigators will include older men and women with a wide age range and of varying health status. Outcomes include health related quality of life, muscle strength, executive cognitive function and cardiovascular events, with a minimum of 1 year of follow up. Blood and urine samples will be stored in a biobank, to allow future research on causes of ill health in older people with SCH.

The investigators have the support of patient advocacy groups and a consortium with the wide range of expertise and experience required to conduct large scale multicentre clinical trials. The proposal explores the multisystem and quality of life benefits to older people of a tailored approach to management of SCH.

This clinical trial should definitively clarify whether thyroxine treatment for SCH provides benefits that are relevant for patients. This trial will provide strong evidence with the potential to improve clinical practice, reduce health care costs and promote healthy ageing of older adults.

Enrollment

737 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Community-dwelling patients aged >=65 years with Subclinical Hypothyroidism (SCH).

SCH is defined as elevated TSH levels (>=4.6, <=19.9 mU/L) and free thyroxine (fT4) in reference range measured on a minimum of two occasions at least 3 months apart.

Exclusion criteria

Subjects currently on Levothyroxine or antithyroid drugs, amiodarone or lithium.
Recent thyroid surgery or radio-iodine (within 12 months).
Grade IV NYHA heart failure.
Prior clinical diagnosis of dementia.
Recent hospitalisation for major illness or elective surgery (within 4 weeks).
Recent acute coronary syndrome, including myocardial infarction or unstable angina (within 4 weeks).
Terminal illness.
Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption.
Subjects who are participating in ongoing RCTs of therapeutic interventions (including CTIMPs)
Plan to move out of the region in which the trial is being conducted within the next 2 years (proposed minimum follow-up period).