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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01023152
Other study ID # 4-2008-0423
Secondary ID
Status Completed
Phase N/A
First received December 1, 2009
Last updated December 1, 2009

Study information

Verified date December 2009
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority South Korea: Korea Food and Drug Administration (KFDA)
Study type Interventional

Clinical Trial Summary

The purpose of this study is to study the effect of remote ischemic preconditioning on acute kidney injury in patients undergoing heart valve replacement surgery with cardiopulmonary bypass.


Description:

Hypothesis : RIPC using tourniquet might be a simple technique with the benefit to provide renal protection without disturbing operating procedure and prolongation of total operating time.


Recruitment information / eligibility

Status Completed
Enrollment 74
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- patients undergoing complex valve surgery.

Exclusion Criteria:

- older than 80 years

- those with left main disease >50%, or hepatic or pulmonary disease

- active infective endocarditis

- left ventricular ejection fraction <30%

- myocardial infarction (MI) within 3 weeks

- pre-existing renal dysfunction (serum creatinine (Cr) level >1.4 mg/dl), and those with peripheral vascular disease affecting the lower limbs.

Study Design

Intervention Model: Parallel Assignment, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Procedure:
Automated cuff-inflator
RIPC protocol consisted of three 10-min cycles of lower limb ischemia at an inflation pressure of 250 mmHg induced by an automated cuff-inflator placed on the upper leg with an intervening 10 min of reperfusion during which the cuff was deflated.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University
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