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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01930305
Other study ID # NXKJGG2012
Secondary ID
Status Completed
Phase N/A
First received July 17, 2013
Last updated July 10, 2014
Start date June 2012
Est. completion date January 2014

Study information

Verified date July 2014
Source General Hospital of Ningxia Medical University
Contact n/a
Is FDA regulated No
Health authority China: Ministry of Science and Technology
Study type Observational

Clinical Trial Summary

To inversitage whether routine warming of blood is harmful to brain fuction of sugical patients receiving massive transfusion.


Description:

Hypothermia is an effective therapeutic intervention to reduce hypoxic ischemia brain injury in animal experiments and in clinics.In a recent study, it has been shown that perioperative warming was associated with a higher incidence of cognitive dysfunction in elderly patients.Therefore, we hypothesised that perioperative heating transfusion have a side effect on brain function of surgical patients.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date January 2014
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- adult patients scheduled for major surgery under general anesthesia and they probably need a blood transfusion during the procedure.

Exclusion Criteria:•Patients with a history of stroke, central nervous system disease , metabolic disturbance, psychiatric illness, hearing impairment, drug abuse or unwilling to participate in assessment

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China General Hospital of Ningxia Medical University Yinchuan Ningxia
China Ningxia Medical University Yinchuan Ningxia

Sponsors (1)

Lead Sponsor Collaborator
General Hospital of Ningxia Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Other serum concentration of inflammatory cytokine change from baseline at 3hour, 6hour, 12hour, 24hour after transfusion Yes
Primary Brain fuction during perioperative period Brain function includes cerebral blood flow and cerebral oxygen saturation Change from baseline at post-transfusion 15min, 30min, 1hour, 2hour, 3 hour, 6hour, 12hour, 24hour Yes
Secondary the cognitive performance and the score of postoperative quality recovery scales ( PQRS) Chang from baseline at 15min,40min,1day,3day and 7day postoperative lay Yes
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