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Effect of Remote Ischemic Perconditioning on Acute Kidney Injury in Adult Valve Replace

Effect of Remote Ischemic Perconditioning on Acute Kidney Injury in Adult Valve Replace

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01476969
Enrollment
90
Registered
2011-11-22
Start date
2011-09-30
Completion date
2012-11-30
Last updated
2012-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic Reperfusion Injury, Rheumatic Disease of Heart Valve

Keywords

Ischemia reperfusion injury, Cardiopulmonary bypass, Remote Ischemic Postconditioning, Other Functional Disturbances Following Cardiac Surgery

Brief summary

The purpose of this study is to determine whether Remote Ischemic Perconditioning is effective on Acute kidney injury in adult valve replacement.

Detailed description

Methods: Patients meeting the requirement will be randomized into 2 groups: the treatment group consisted of three 5-minute cycles left lower limb ischemia, induced by inflating a blood pressure cuff on the lower limb to 600 mmHg with an intervening 5 minutes of reperfusion, during which time the cuff was deflate; the control group consisted of placing an uninflated cuff on the left lower limb for 30 minutes. The postconditioning protocol was applied after the aortic cross-clamping. The clinical data of inotropes requirement, drainage, ventilation and intensive care time will be recorded. Venous blood samples will be taken perioperatively for detecting concentration of troponin I (cTnI), Myocardial enzyme, Renal function, Cystatin c, and High-sensitivity c-reactive protein(HS-CRP).

Interventions

the treatment group consisted of three 4-minute cycles left lower limb ischemia,induced by inflating a blood pressure cuff on the lower limb to 600 mmHg with an intervening 4 minutes of reperfusion ,during which time the cuff was deflate;the control group consisted of placing an uninflated cuff on the left lower limb for 24 minutes.The postconditioning protocol was applied after the aortic cross-clamping.

Sponsors

Central South University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* rheumatic heart valve disease requiring selective aortic or double valve(aortic and mitral valve) replacement

Exclusion criteria

* infective endocarditis congenital valve disease previous cardiac surgery complicated with rereplace valve * Renal dysfunction * diabetes * coronary artery disease * hypertension * peripheral vascular disease affecting the lower limb free of arteriovenous fistula * receiving aspirin, corticosteroids, angiotensin-converting enzyme inhibitors or statin perioperatively

Design outcomes

Primary

MeasureTime frame
Renal functionwithin the first 48h after cardiac surgery

Secondary

MeasureTime frame
concentration of troponin I (cTnI)within 48h after cardiac surgery
Myocardial enzymewithin 48h after cardiac surgery
Cystatin Cwithin 48h after cardiac surgery
High-sensitivity c-reactive protein(HS-CRP)within 48h after cardiac surgery

Countries

China

Contacts

Primary ContactLuo Wanjun, M.D.
luo3478@yahoo.cn86-731-89753503
Backup ContactLv Hongwei, M.D.
hongweilv@163.com86-13467616975

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026