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Clinical Trial Details — Status: Not yet recruiting

Administrative data

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

Study information

Verified date September 2005
Source Rambam Health Care Campus
Contact Shlomo Keidar, MD
Phone 97248542518
Email skeidar@rambam.health.gov.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Educational/Counseling/Training


Related Conditions & MeSH terms


Intervention

Drug:
candesartan


Locations

Country Name City State
Israel Internal Ward "A", Rambam Medical Center Haifa

Sponsors (1)

Lead Sponsor Collaborator
Rambam Health Care Campus

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary ACE and ACE2 activities in monocytes
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