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Desiccated Thyroid Extract and Levothyroxine for Hypothyroidism Treatment

Desiccated Thyroid Extract Compared to Levothyroxine in the Treatment of Hypothyroidism: A Randomized, Double-blind, Crossover Study.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01739972
Acronym
DTE
Enrollment
180
Registered
2012-12-04
Start date
2012-05-31
Completion date
2014-05-31
Last updated
2012-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Hypothyroidism.

Keywords

Desiccated thyroid extract and levothyroxine

Brief summary

Our hypothesis is that hypothyroid patients on DTE may have a decrease in symptoms, an improvement of cognitive function, and an increase in sense of well-being/ quality of life equivalently compared with L-T4.

Interventions

DRUGLevothyroxine

Levothyroxine in a capsule form, once daily, with appropriate dosage to keep TSH in the normal range.

Armour thyroid in a capsule form, once daily, with appropriate dosage to keep TSH in normal range.

Sponsors

Walter Reed National Military Medical Center
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients will be between the ages of 18 to 65 and will have been on levothyroxine for primary hypothyroidism for at least 6 months.

Exclusion criteria

* Patients will be excluded if they have the following problems: pregnancy, plan for pregnancy in the next 12 months, cardiac disease, especially coronary artery disease, chronic obstructive lung disease, malabsorption disorder, gastrointestinal surgeries, significant renal or liver dysfunction, seizure disorders, thyroid and non-thyroid active cancers, uncontrolled psychosis, psychotropic medication use, steroid use, amiodarone, chemotherapy for cancer, iron supplement more than 325mg per day, carafate/ proton pump inhibitor use, cholestyramine use, and those with recent PCS orders who are expected to move out of the geographic area, age less than 18 years old or older than 65 years old. * Patients scheduled for deployment will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
thyroid-symptom questionnaire4 monthsThyroid Symptom Questionnaire, a health-related quality-of-life questionnaire, that consists of 12 questions, presented in the same format as the GHQ-12, that asked patients how they felt over the last three months.
Wechsler Memory Scale-Version IV (WMS-IV)4 monthsThe Wechsler Memory Scale-Version IV (WMS-IV) included auditory memory index, visual memory index, visual working memory index, immediate memory index and delayed memory index.

Secondary

MeasureTime frameDescription
Biochemical measures4 monthsBiochemical testing consisting of serum TSH, free T4, total T4, total T3, T3 resin uptake, sex hormone binding globulin (SHBG), and a lipid panel.

Other

MeasureTime frameDescription
Beck Depression Index4 monthsThe BDI is a self-rating scale of 21 items, in which scores of 10 or less indicate normal mood variation and scores of 11 or more reflect increasing levels of depression. Clinically important depression is associated with scores of 20 or more.
General health questionnaire-124 monthsGeneral health questionnaire - consists of 12 quality of life questions.
Clinical preference4 monthsAt the completion of the study, each patient will be asked which treatment (the first or the second) he or she preferred.

Countries

United States

Contacts

Primary ContactMohamed KM Shakir, MD
mohamed.k.shakir.civ@health.mil301-295-5165
Backup ContactPatrick W Clyde, MD
patrick.w.clyde.mil@health.mil301-295-5165

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026