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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02756715
Other study ID # KUH1160100
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 30, 2016
Est. completion date February 27, 2020

Study information

Verified date February 2020
Source Konkuk University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Ischeic reperfusion injury lead to a cellular dyfunction and increase in soluble glycocalyx of blood flow. syndecan-1 was a marker of glycocalyx.

The purpose of this study is to prove the variation of level of serum syndecan-1 between preoperative and postoperative period.


Description:

The patients were allocated randomly to receive propofol or desflurane. Also, a total of 6ml of blood sample was obtained for total 6 times in consecutive order.

1. Preoperation (immediate before anesthesia induction)

2. Immediate before tourniquet off

3. 5 min after tourniquet off

4. PACU

5. postoperative 6 hours

6. postoperative 24 hours

Serum in blood will be obtained and level of serum cytokine will be evaluated by enzyme-linked immunosorbent assay


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date February 27, 2020
Est. primary completion date March 26, 2018
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- patients who was planned to undergo knee surgery.

Exclusion Criteria:

- age < 20 years old

- history of previous cancer

- history of previous peripheral vascular disease

- Emergency surgery

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
propofol group
Patient will be anesthetized by using propofol infusion during operation.
Desflurane group
Patient will be anesthetized by using desflurane inhalation during operation.

Locations

Country Name City State
Korea, Republic of Konkuk University Medical Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
Konkuk University Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Syndecan-1 change of level of syndecan-1 (scores range from 0 to 100) Preoperative time, Immediate before tourniquet off,5 min after tourniquet off,PACU, postoperation after 6hours, postoperation after 24hours
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