Dosing of LT4 in Older Individuals

Description

Our overall goal is to determine the clinical consequences of allowing greater flexibility in LT4 dosing in older individuals who take LT4.

Conditions

Hypothyroidism

Study Overview

Study Details

Study overview

Our overall goal is to determine the clinical consequences of allowing greater flexibility in LT4 dosing in older individuals who take LT4.

Levothyroxine Dosing in Older Individuals

Dosing of LT4 in Older Individuals

Condition
Hypothyroidism
Intervention / Treatment

-

Contacts and Locations

Philadelphia

Penn Medicine, Smilow Translational Research Center, Philadelphia, Pennsylvania, United States, 19104

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Provision of signed and dated informed consent form
  • 2. Stated willingness to comply with all study procedures and availability for the duration of the study
  • 3. Male or female, community dwelling, aged 65 years or older
  • 4. Diagnosed with hypothyroidism of any etiology for at least 6 months, taking 75-200 mcg per day LT4 and a minimum of 1.2 mcg/kg/day with no dose adjustment since the last TSH test.
  • 5. Ability to take oral medication and be willing to adhere to the medication regimen
  • 1. Hypopituitarism
  • 2. History of thyroid cancer requiring suppression of TSH secretion
  • 3. Current use of liothyronine (LT3), thyroid extracts, Tirosint liquid or capsules, and medications that interfere with thyroid function or thyroid function tests
  • 4. GFR \<30 ml/min/1.73 m2 within the prior 12 months
  • 5. Unable to understand and comply with study requirements, as assessed by study staff and the PI, will be excluded.
  • 6. Other conditions which, in the opinion of the investigators, would prevent them from participating in the full duration of the study.

Ages Eligible for Study

65 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Pennsylvania,

Anne R. Cappola, M.D., Sc.M., PRINCIPAL_INVESTIGATOR, University of Pennsylvania

Study Record Dates

2028-04-01