Trial · NCT00106119
Thyroid and Glucose and Energy Metabolism
NCT00106119, Phase 2, Completed, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); results first posted 2015-02-23
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Thyroid and Glucose and Energy Metabolism. Trials, record NCT00106119. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00106119
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Thyroid and Glucose and Energy Metabolism
- NCT number
- NCT00106119
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 18 participants, actual
- Lead sponsor
- National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
- Conditions
- Thyroid Diseases
- Interventions
- Liothyronine and Levothyroxine
- First posted
- 2005-03-21
- Last updated
- 2015-02-23
- Results first posted
- 2015-02-23
Source ClinicalTrials.gov
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Insulin-mediated Glucose Disposal Rate at Levothyroxine Treatment Phase | One month of therapy. | |
| Primary | Insulin-mediated Glucose Disposal Rate at Liothyronine Treatment Phase | One month of therapy | |
| Secondary | Total Cholesterol at Levothyroxine Treatment Phase | One month of therapy. | |
| Secondary | Total Cholesterol at Liothyronine Treatment Phase | One month of therapy. | |
| Secondary | Triglycerides at Levothyroxine Treatment Phase | One month of therapy. | |
| Secondary | Triglycerides at Liothyronine Treatment Phase | One month of therapy. | |
| Secondary | Resting Energy Expenditure at Levothyroxine Treatment Phase | One month of therapy. | |
| Secondary | Resting Energy Expenditure at Liothyronine Treatment Phase | One month of therapy. | |
| Secondary | Left Ventricle Mass Index at Levothyroxine Treatment Phase | One month of therapy. | |
| Secondary | Left Ventricle Mass Index at Liothyronine Treatment Phase | One month of therapy. |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 registered outcomesOutcomes14
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Insulin-mediated Glucose Disposal Rate at Levothyroxine Treatment Phase | One month of therapy. | mg/kg/min | MEAN | |
| SECONDARY | Total Cholesterol at Levothyroxine Treatment Phase | One month of therapy. | mg/dl | MEAN | |
| PRIMARY | Insulin-mediated Glucose Disposal Rate at Liothyronine Treatment Phase | One month of therapy | mg/kg/min | MEAN | |
| SECONDARY | Total Cholesterol at Liothyronine Treatment Phase | One month of therapy. | mg/dl | MEAN | |
| SECONDARY | Triglycerides at Levothyroxine Treatment Phase | One month of therapy. | mg/dl | MEAN | |
| SECONDARY | Triglycerides at Liothyronine Treatment Phase | One month of therapy. | mg/dl | MEAN | |
| SECONDARY | Resting Energy Expenditure at Levothyroxine Treatment Phase | One month of therapy. | kcal/24 hour | MEAN | |
| SECONDARY | Resting Energy Expenditure at Liothyronine Treatment Phase | One month of therapy. | kcal/24 hour | MEAN | |
| SECONDARY | Left Ventricle Mass Index at Levothyroxine Treatment Phase | One month of therapy. | g/m^2 | MEAN | |
| SECONDARY | Left Ventricle Mass Index at Liothyronine Treatment Phase | One month of therapy. | g/m^2 | MEAN |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 outcomesResults by group14
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Insulin-mediated Glucose Disposal Rate at Levothyroxine Treatment Phase | Liothyronine/Levothyroxine Therapy Intervention Arm | 7.26 | Standard Deviation 2.7 | mg/kg/min | |
| Total Cholesterol at Levothyroxine Treatment Phase | Liothyronine/Levothyroxine Therapy Intervention Arm | 196 | Standard Deviation 26 | mg/dl | |
| Insulin-mediated Glucose Disposal Rate at Liothyronine Treatment Phase | Liothyronine/Levothyroxine Therapy Intervention Arm | 7.37 | Standard Deviation 4.4 | mg/kg/min | |
| Total Cholesterol at Liothyronine Treatment Phase | Liothyronine/Levothyroxine Therapy Intervention Arm | 174 | Standard Deviation 28 | mg/dl | |
| Triglycerides at Levothyroxine Treatment Phase | Liothyronine/Levothyroxine Therapy Intervention Arm | 152 | Standard Deviation 31 | mg/dl | |
| Triglycerides at Liothyronine Treatment Phase | Liothyronine/Levothyroxine Therapy Intervention Arm | 144 | Standard Deviation 16 | mg/dl | |
| Resting Energy Expenditure at Levothyroxine Treatment Phase | Liothyronine/Levothyroxine Therapy Intervention Arm | 1201 | Standard Deviation 282 | kcal/24 hour | |
| Resting Energy Expenditure at Liothyronine Treatment Phase | Liothyronine/Levothyroxine Therapy Intervention ArmArm | 1177 | Standard Deviation 323 | kcal/24 hour | |
| Left Ventricle Mass Index at Levothyroxine Treatment Phase | Liothyronine/Levothyroxine Therapy Intervention Arm | 71 | Standard Deviation 16 | g/m^2 | |
| Left Ventricle Mass Index at Liothyronine Treatment Phase | Liothyronine/Levothyroxine Therapy Intervention Arm | 71 | Standard Deviation 19 | g/m^2 |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 results by groupParticipant flow18
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| First Intervention | STARTED | Liothyronine First, Then Levothyroxine | 7 | |
| First Intervention | STARTED | Levothyroxine First, Then Liothyronine | 7 | |
| First Intervention | COMPLETED | Liothyronine First, Then Levothyroxine | 7 | |
| First Intervention | COMPLETED | Levothyroxine First, Then Liothyronine | 7 | |
| First Intervention | NOT COMPLETED | Liothyronine First, Then Levothyroxine | 0 | |
| First Intervention | NOT COMPLETED | Levothyroxine First, Then Liothyronine | 0 | |
| Washout Period of 30 Days | STARTED | Liothyronine First, Then Levothyroxine | 7 | |
| Washout Period of 30 Days | STARTED | Levothyroxine First, Then Liothyronine | 7 | |
| Washout Period of 30 Days | COMPLETED | Liothyronine First, Then Levothyroxine | 7 | |
| Washout Period of 30 Days | COMPLETED | Levothyroxine First, Then Liothyronine | 7 |
1 to 10 of 18Source ClinicalTrials.gov
See all 18 participant flowAdverse events4
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | generalized anxiety disorder | Psychiatric disorders | Levothyroxine Period | 1 | 14 | 14 |
| other | generalized anxiety disorder | Psychiatric disorders | Liothyronine Period | 0 | 14 | 0 |
| serious | General disorders | General disorders | Levothyroxine Period | 0 | 14 | 0 |
| serious | General disorders | General disorders | Liothyronine Period | 0 | 14 | 0 |
Source ClinicalTrials.gov
Adverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Levothyroxine Period | ||
| Total, all-cause mortality | Liothyronine Period | ||
| Total, other adverse events | Levothyroxine Period | 1 | 14 |
| Total, other adverse events | Liothyronine Period | 0 | 14 |
| Total, serious adverse events | Levothyroxine Period | 0 | 14 |
| Total, serious adverse events | Liothyronine Period | 0 | 14 |
Source ClinicalTrials.gov
Papers6
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons1
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison |
|---|
| Levothyroxine Period vs Liothyronine Period: serious adverse events |
Source Trial comparisons
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT00106119
GET https://conductscience.org/api/trials/v1/NCT00106119/registered