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To determine whether treatment with the ENaC inhibitor, amiloride, improves endothelial function and arterial stiffness in obese insulin resistant subjects in a randomized placebo-controlled trial examining pre and postmenopausal women and age-matched men.
Overweight/obese males, pre- and post-menopausal females with insulin resistance, 30-70 years of age will be recruited. Following screening, eligible men and women will be randomly assigned to either amiloride (max dose 5mg) or placebo in a double-blinded design manner.
After randomization, subjects will be scheduled for an outpatient visit to the undergo baseline assessment of arterial stiffness (carotid femoral pulse wave velocity - cfPWV) and endothelial function (brachial popliteal artery flow mediated dilation). Subject assessment will be repeated at 12 weeks and at 24 weeks.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo | Placebo Comparator | 6 months of daily placebo |
|
| Amiloride | Experimental | 6 months of amiloride (max dose 5 mg) treatment |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Placebo - Cap | Drug | 6 months of 1 pill a day |
| |
| Amiloride Pill |
| Measure | Description | Time Frame |
|---|---|---|
| Carotid Femoral Pulse Wave Velocity | cfPWV is the gold standard of arterial stiffness. It was assessd during experimental visits, under the same conditions in a blinded manner | baseline, 3 and 6 mo |
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| Measure | Description | Time Frame |
|---|---|---|
| Systolic Blood Pressure | Systolic blood pressure obtained during experimental visits at the different time points | 3 and 6 mo |
| Brachial Artery Flow Mediated Dilation (FMD) | Brachial artery flow-mediated dilation will be assessed at baseline, 12, and 24 weeks. FMD is a measurement of conduit artery endothelial function. |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Camila Manrique Acevedo, MD | University of Missouri-Columbia | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Missouri Hospital and Clinics | Columbia | Missouri | 65201 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Placebo | 6 months of daily placebo Placebo - Cap: 6 months of 1 pill a day |
| FG001 | Amiloride | 6 months of amiloride (max dose 5 mg) treatment Amiloride Pill: Max dose of 5 mg a day for 6 months |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Placebo | 6 months of daily placebo Placebo - Cap: 6 months of 1 pill a day |
| BG001 | Amiloride | 6 months of amiloride (max dose 5 mg) treatment Amiloride Pill: Max dose of 5 mg a day for 6 months |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Other Pre-specified | Systolic Blood Pressure | Systolic blood pressure obtained during experimental visits at the different time points | Posted | Mean | 95% Confidence Interval | mmHg | 3 and 6 mo |
|
|
6 months
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Placebo | 6 months of daily placebo Placebo - Cap: 6 months of 1 pill a day | 0 |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Headache | Nervous system disorders | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Camila Manrique, MD | University of Missouri | 573-882-2554 | manriquec@missouri.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Oct 30, 2023 | Sep 22, 2025 | Prot_001.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Nov 13, 2025 | Nov 17, 2025 | SAP_003.pdf |
| ICF | No | No | Yes | Informed Consent Form | Nov 9, 2023 | Jul 11, 2025 | ICF_000.pdf |
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| ID | Term |
|---|---|
| D050177 | Overweight |
| D009765 | Obesity |
| D007333 | Insulin Resistance |
| ID | Term |
|---|---|
| D044343 | Overnutrition |
| D009748 | Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
| D001835 | Body Weight |
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| ID | Term |
|---|---|
| D000584 | Amiloride |
| ID | Term |
|---|---|
| D011719 | Pyrazines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
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| Drug |
Max dose of 5 mg a day for 6 months |
|
| Baseline, 3 months (interim) and 6 months (final) |
| Popliteal Artery Flow Mediated Dilation (FMD) | Popliteal artery flow-mediated dilation will be assessed at baseline, 12, and 24 weeks. FMD is a measurement of conduit artery endothelial function. | Baseline, 3 months (interim) and 6 months (final) |
| Physician Decision |
|
| Lost to Follow-up |
|
| BG002 | Total | Total of all reporting groups |
| Participants |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Participants |
|
|
| Other Pre-specified | Brachial Artery Flow Mediated Dilation (FMD) | Brachial artery flow-mediated dilation will be assessed at baseline, 12, and 24 weeks. FMD is a measurement of conduit artery endothelial function. | Posted | Mean | 95% Confidence Interval | Percentage | Baseline, 3 months (interim) and 6 months (final) |
|
|
|
| Other Pre-specified | Popliteal Artery Flow Mediated Dilation (FMD) | Popliteal artery flow-mediated dilation will be assessed at baseline, 12, and 24 weeks. FMD is a measurement of conduit artery endothelial function. | Posted | Mean | 95% Confidence Interval | Percentage | Baseline, 3 months (interim) and 6 months (final) |
|
|
|
| Primary | Carotid Femoral Pulse Wave Velocity | cfPWV is the gold standard of arterial stiffness. It was assessd during experimental visits, under the same conditions in a blinded manner | Number of participants that finished clinical trial | Posted | Mean | 95% Confidence Interval | m/s | baseline, 3 and 6 mo |
|
|
|
| 47 |
| 0 |
| 47 |
| 5 |
| 47 |
| EG001 | Amiloride | 6 months of amiloride (max dose 5 mg) treatment Amiloride Pill: Max dose of 5 mg a day for 6 months | 0 | 90 | 0 | 90 | 9 | 90 |
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| D012816 |
| Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D006946 | Hyperinsulinism |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |