Increased Renal Oxygenation and Angiotensin Converting Enzyme Inhibition
This study has been completed.
Sponsor:
Instituto de Cardiologia do Rio Grande do Sul
Information provided by (Responsible Party):
Maria Antonieta Moraes, Instituto de Cardiologia do Rio Grande do Sul
ClinicalTrials.gov Identifier:
NCT01545479
First received: January 16, 2012
Last updated: March 1, 2012
Last verified: March 2012
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Purpose
It is well established that renal hypoxia is associated with the development of renal injury. The purpose of this study is measure the alterations in renal blood oxygenation after angiotensin II converting enzyme inhibition. The understanding of kidney adaptive mechanisms to renin angiotensin system effects in healthy subjects will be useful for the early detection of renal disease and for the development of new therapies to decrease the progression of the disease and its consequences.
| Condition | Intervention | Phase |
|---|---|---|
|
Renal Disease |
Drug: captopril 25mg |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Health Services Research |
| Official Title: | Renal Oxygen Content is Increased in Healthy Subjects After Angiotensin Converting Enzyme Inhibition |
Resource links provided by NLM:
Further study details as provided by Instituto de Cardiologia do Rio Grande do Sul:
Primary Outcome Measures:
- Measure the renal blood oxigenation after angiotensin converting enzyme inhibition [ Time Frame: up to 12 months ] [ Designated as safety issue: Yes ]
| Enrollment: | 5 |
| Study Start Date: | January 2010 |
| Study Completion Date: | December 2010 |
| Primary Completion Date: | October 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Captopril 25mg
To study the renal blood oxygenation, the subjects took captopril (25mg).
|
Drug: captopril 25mg
renal blood oxygenation after captopril
Other Name: BOLD-MRI
|
Show Detailed Description
Eligibility| Ages Eligible for Study: | 45 Years to 55 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- healthy female between 45 and 55 years
Exclusion Criteria
- man and
- health female below 45 and above 55 years
Contacts and Locations
More Information
No publications provided by Instituto de Cardiologia do Rio Grande do Sul
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Maria Antonieta Moraes, Doctorate, Instituto de Cardiologia do Rio Grande do Sul |
| ClinicalTrials.gov Identifier: | NCT01545479 History of Changes |
| Other Study ID Numbers: | 4111/08 |
| Study First Received: | January 16, 2012 |
| Last Updated: | March 1, 2012 |
| Health Authority: | Brazil: Ethics Committee |
Keywords provided by Instituto de Cardiologia do Rio Grande do Sul:
|
ECA BOLD-MRI kidney |
Additional relevant MeSH terms:
|
Kidney Diseases Urologic Diseases Captopril Angiotensin-Converting Enzyme Inhibitors Protease Inhibitors Enzyme Inhibitors |
Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Antihypertensive Agents Cardiovascular Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 19, 2013