Role of Mineralocorticoid Receptor in Diabetic Cardiovascular Disease
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials
| City: |
|
Boston |
| State: |
|
Massachusetts |
| Zip Code: |
|
02115 |
| Conditions: |
|
Type 2 Diabetes Mellitus - Vascular Disease |
| Purpose: |
|
Aldosterone is a significant mediator of cardiovascular injury associated with heart failure
and the cardiovascular benefits of mineralocorticoid receptor blockade are additive to those
of angiotensin converting enzyme inhibitors or angiotensin II receptor blockers. This study
will test the hypothesis that MR antagonists exert beneficial cardiovascular effects,
specifically by decreasing vascular injury and improving vascular function.A randomized,
double-blind study will be conducted, in which subjects with Type 2 Diabetes Mellitus will
undergo a series of assessments to test heart, blood vessel, and kidney function at
baseline, and after 2 and 6 months of treatment with one of the following drugs:
1. spironolactone
2. hydrochlorothiazide plus potassium
3. placebo.
In the event of insufficient funds, randomization to the placebo arm will be stopped and
primary assessment of outcomes will occur at baseline and after 6 months of treatment.
|
| Study Summary: |
|
|
| Criteria: |
|
Inclusion Criteria:
- age 18-70 years
- type 2 diabetes mellitus
- with or without hypertension
Exclusion Criteria:
- ischemic changes on resting electrocardiogram,
- clinical evidence of heart disease (angina, heart failure, unstable
angina),cerebrovascular or peripheral vascular disease,
- significant cardiac arrhythmias,
- aortic stenosis,
- 2nd or 3rd degree atrio-ventricular block, sinus node disease, or symptomatic
bradycardia,
- bronchospastic lung disease with active wheezing,
- known hypersensitivity to adenosine,
- hemoglobin A1C > 8.5%, *
- gout (If not already taking HCTZ),
- the use of Rosiglitazone,**
- eGFR < 60 ml/min,
- serum potassium > 5.0 mmol/L,
- use of potassium-sparing diuretics,**
- current smoker,*
- pregnancy,
- renal disease not related to diabetes mellitus,
- uncontrolled hypertension, systolic BP >160 mm Hg and diastolic BP >100 mm Hg,*
- use of cyclic hormone replacement therapy
- past intolerance of ACE inhibitor therapy
- other major medical illnesses. Subjects with evidence of a previous myocardial
infarction on the first adenosine-stimulated PET study will be withdrawn from the
study.
- Screening systolic blood pressure < 105 mm Hg off of anti-hypertensive medications
- Subjects can enroll in study and proceed with in-patient evaluations if during
the run-in period adjustments of medications, diet and habits lead to improved
glucose control (equivalent to HbA1c <8.5%), controlled hypertension and
cessation of smoking.
- Subjects who are currently taking these medications will not qualify for a
screening visit. If medications were recently stopped by the subject's
physician, he or she may be screened but the baseline assessment protocol
must occur 3 months after stopping.
|
| NCT ID: |
|
NCT00865124 |
| Primary Contact: |
|
Principal Investigator
Gail K Adler, MD, PhD
Brigham and Women's Hospital
|
| Backup Contact: |
|
N/A |
| Location Contact: |
|
Boston, Massachusetts 02115
United States
There is no listed contact information for this specific location.
Site Status: N/A |
| Data Source: |
|
ClinicalTrials.gov |
| Date Processed: |
|
June 18, 2013 |
| Modifications to this listing: |
|
Only selected fields are shown, please use the link
below to view all information about this clinical trial. |
|
Click to view Full Listing
|