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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01584570
Other study ID # 4-2011-0791
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2012
Est. completion date December 23, 2013

Study information

Verified date February 2019
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate effect of dexmedetomidine and tracheal intubation on heart rate variability and QTc interval.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 23, 2013
Est. primary completion date December 23, 2013
Accepts healthy volunteers No
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- patient who are regarded as ASA class I

- age 20 to 60

- patient scheduled for Intubation for surgery

Exclusion Criteria:

- QTc interval > 440 ms

- arrythmia

- Patient who is taking a medicine which effects QTc interval

- HTN

- DM

- renal disease

- hepatic disease

- pregnant

- illiterate

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
0.5 mcg/kg IV infusion for 10 min, 1.0 mcg/kg IV infusion for 10 min
ECG monitoring for evaluation of QTc interval

Locations

Country Name City State
Korea, Republic of Severance hospital 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 Change of QTc interval T1- baseline, T2- to evaluate the effect of dexmedetomidine on QTc interval, T3- to evaluate QTc interval just before intubation, T4,5,6 - to evaluate QTc interval after intubation T1 (at rest), T2 (5 min after dexmedetomidine infusion), T3 (just before intubation), T4(1 min after intubation), T5(2 min after intubation), T6(3min after intubation)
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