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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01921595
Other study ID # 4-2013-0350
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date August 2013
Est. completion date January 31, 2015

Study information

Verified date December 2015
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of study is to compare the effect of coagulation profile in patients receiving intraoperative balanced salt colloid undergoing spinal cord tumor surgery.


Recruitment information / eligibility

Status Terminated
Enrollment 6
Est. completion date January 31, 2015
Est. primary completion date January 31, 2015
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- adult patients over the age of 20 scheduled for spinal tumor removal and fixation

Exclusion Criteria:

- 1. Renal failure 2. Preexisting congestive heart failure(NYHA III ~ IV) 3. Anemia 4. Coagulopathy 5. Abnormal liver function 6. Anti coagulation/Anti platelet ,edication 7. Foreigner, illiterate 8. Disabled person,

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Valanced salt colloid
Maximum dose : 30ml/kg, IV, The infusion of valanced salt colloid is started at bleeding and continued until reach at maximum dose
Valanced salt crystalloid group
Maximum dose : 30ml/kg, IV, The infusion of valanced salt crystalloid is started at bleeding and continued until reach at maximum dose

Locations

Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Compare the effect of coagulation profile in patients receiving intraoperative balanced salt colloid undergoing spinal cord tumor surgery. ROTEM, CBC, PT/aPTT,ABGA, Lactic acid, electrolyte up to 24hrs after anesthesia induction
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