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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00693498
Other study ID # 24518
Secondary ID
Status Completed
Phase N/A
First received June 5, 2008
Last updated January 4, 2018
Start date July 2008
Est. completion date November 2009

Study information

Verified date January 2018
Source University of Rochester
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Background: Children having open heart surgery to repair congenital heart defects demonstrate a large inflammatory response to the heart-lung machine and to surgery itself. In general, the more intense their inflammatory response, the more critically ill they are following surgery. These children routinely require large numbers of blood transfusions during and following surgery as part of their medical management that adds to their heightened inflammatory state. Whether additional steps to "wash" blood products and remove the substances contributing to post-transfusion inflammation will limit this response, and improve the health of children following open heart surgery, remains to be studied.

Aims: To compare the inflammatory response in children having open heart surgery who receive washed versus unwashed blood transfusions.

Methods: We will randomly assign children having open heart surgery to one of two groups: group 1 will receive blood transfusions per the current standard of care, group 2 will receive blood transfusions that have been washed in addition to the current standard of care. We will then use blood tests to measure the inflammatory response in children of each group. We will compare the results to determine whether washing blood transfusions decreases inflammation and post-operative complications following open heart surgery.

Conclusion: We believe that washing blood transfusions given to children following open heart surgery will decrease their inflammatory response and improve their overall health.


Recruitment information / eligibility

Status Completed
Enrollment 162
Est. completion date November 2009
Est. primary completion date November 2009
Accepts healthy volunteers No
Gender All
Age group N/A to 17 Years
Eligibility Inclusion Criteria:

1. age < 18 years

2. surgical repair at URMC by the pediatric cardiac surgical team

3. informed consent signed by the parent or legal guardian, and if applicable, assent obtained from the subject.

Exclusion Criteria:

1. Age =18 years

2. inability to provide consent/assent; 3) subjects having "emergent" surgical procedures. Subjects with chronic inflammatory or autoimmune disorders will not be excluded

Study Design


Intervention

Biological:
Standard leukoreduced irradiated blood cell transfusion
standard vs washed blood cell transfusions
Washed leukoreduced irradiated blood cell transfusions
washed leukoreduced irradiated blood cell transfusions

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Rochester

Outcome

Type Measure Description Time frame Safety issue
Primary 12 Hour Plasma Interleukin (IL)-6 to IL-10 Ratio plasma was obtained pre-op, immediately once off cardiopulmonary bypass (CPB), six hours following CPB and 12 hours following CPB. The plasma was centrifuged and the supernatant collected and stored at -70 degrees. The samples then underwent Luminex testing for IL-6 and IL-10 levels, and the IL-6:IL-10 ratio was calculated (IL-6 being the numerator and IL-12 being the denominator). The 12 hour ratio was the primary outcome measure. 12 hours post-cardiopulmonary bypass
Secondary Median wrCRP Level wide range C reactive protein levels were obtained before surgery (pre-operatively) and on post-operative day 1 and 2 in transfused subjects post op day 1 and 2
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