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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02001298
Other study ID # HJKim3
Secondary ID
Status Completed
Phase N/A
First received November 24, 2013
Last updated December 3, 2013
Start date June 2012

Study information

Verified date November 2013
Source Jeju National University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is the comparison of the cardiovascular effects of remifentanil and nitroprusside for controlled hypotension


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date
Est. primary completion date July 2013
Accepts healthy volunteers No
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- Patients who underwent endoscopic sinus surgery

Exclusion Criteria:

- patient who took any drug to influence this study

- patient with cardiovascular disease, renal disease or liver disease

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
remifentanil

nitroprusside


Locations

Country Name City State
Korea, Republic of Jeju National University Hospital Jeju-si Jeju Special Self-Governing Province

Sponsors (1)

Lead Sponsor Collaborator
Jeju National University School of Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Other Stroke volume index Stroke volume index was continuously measured during controlled hypotension using noninvasive cardiac output monitor. The average of stroke volume index during controlled hypotension was compared with baseline value. Stroke volume index was continuously measured during controlled hypotension, an average of 90 min
Primary Cardiac index Cardiac index was continuously measured during controlled hypotension using noninvasive cardiac output monitor. The average of cardiac index during controlled hypotension was compared with baseline value. Cardiac index was continuously measured during controlled hypotension, an average of 90 min
Secondary Total peripheral resistance index Total peripheral resistance index was continuously measured during controlled hypotension using noninvasive cardiac output monitor. The average of total peripheral resistance index during controlled hypotension was compared with baseline value. Total peripheral resistance index was continuously measured during controlled hypotension, an average of 90 min
See also
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