NIDDM Clinical Trial
Official title:
ACE/ACE2 Ratio in Diabetic Patients Treated With Antihypertensive Drugs
NCT number | NCT00192803 |
Other study ID # | ACE2.CTIL |
Secondary ID | |
Status | Not yet recruiting |
Phase | Phase 4 |
First received | September 14, 2005 |
Last updated | February 22, 2006 |
This feasibility study is designed to examine modulation of the relative activities of ACE
and ACE2 in diabetic patients following treatment with the angiotensin type 1 receptor
(AT1R) antagonist, Candesartan.
This study will provide a closer insight to the possible involvement of the
renin-angiotensin system (RAS)-related enzymatic components in development or attenuation of
vascular pathogenesis.
Status | Not yet recruiting |
Enrollment | 20 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 90 Years |
Eligibility |
Inclusion Criteria: - Signed informed consent - Non-smokers - Type II DM diagnosed patients - Blood pressure < 135/90 - Serum HbA1C > 7% - Serum creatinine < 1mg% - Urine microalbumin < 300 mg/day - Body mass index (BMI) < 35 kg/m2 Exclusion Criteria: - Insulin-dependent diabetic patients - Patient with persistent microalbuminuria - Patient with history of severe hypertension - Congestive heart failure - Patient receiving renin-angiotensin-aldosterone system (RAAS)-related anti-hypertensive medications. - Patient with major hepatic disease |
Allocation: Non-Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Educational/Counseling/Training
Country | Name | City | State |
---|---|---|---|
Israel | Internal Ward "A", Rambam Medical Center | Haifa |
Lead Sponsor | Collaborator |
---|---|
Rambam Health Care Campus |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | ACE and ACE2 activities in monocytes |
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