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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01479049
Other study ID # XJXZ2009-1010
Secondary ID
Status Completed
Phase N/A
First received October 7, 2011
Last updated November 23, 2011
Start date October 2009
Est. completion date October 2010

Study information

Verified date November 2011
Source Xijing Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators previously investigated the cardioprotective effect of an adenosine-lidocaine cardioplegia with moderate-potassium (K+, 10.0 mmol/L) in pediatric cardiac surgery, which was associated with better myocardial protective effects when compared with conventional high-potassium cardioplegia. However, this cardioplegia could not be sucked back into the cardiopulmonary bypass (CPB) circuit because of excessive hemodilution and severe systemic hypotension induced by adenosine. Therefore, the investigators supposed that a moderate-potassium (K+, 10.0 mmol/L) blood cardioplegia without adenosine could also arrest the heart and have better myocardial protective effects compared with conventional hyperkalamic cold blood cardioplegia during cardiac operations without excessive hemodilution and systemic hypotension.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date October 2010
Est. primary completion date March 2010
Accepts healthy volunteers No
Gender All
Age group 1 Month to 24 Months
Eligibility Inclusion Criteria:

- pediatric patients (body weight<10 kg)

- congenital heart diseases and scheduled for a repair operation with CPB in the Department of Cardiovascular Surgery, Xijing Hospital.

Exclusion Criteria:

- other systemic diseases

Study Design


Intervention

Drug:
MP (moderate potassium) group
Hearts were arrested with cold blood cardioplegia with moderate potassium concentration (K+, 10mmol/L)during cardiac operation
HP (High potassium) group
Hearts are arrested with cold blood cardioplegia with high potassium concentration (K+, 20mmol/L)during cardiac operation.

Locations

Country Name City State
China Department of Cardiovascular Surgery, Xijing Hospital Xi'an Shaanxi

Sponsors (1)

Lead Sponsor Collaborator
Xijing Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary post-operative Serum cTnI concentration decreased significantly in 24hours myocardial injury could be sensitively reflected by post operative Serum cTnI concentration. 24h after myocardial reperfusion
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