Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01131741
Other study ID # 06-2009-141
Secondary ID
Status Recruiting
Phase N/A
First received May 23, 2010
Last updated February 13, 2011
Start date May 2010
Est. completion date April 2011

Study information

Verified date February 2011
Source Seoul National University Hospital
Contact Jin Huh, MD
Phone 82-2-840-2510
Email huhjin419@gmail.com
Is FDA regulated No
Health authority South Korea: Korea Food and Drug Administration (KFDA)
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether changes in perfusion index can be used for detecting intravascular injection of an epinephrine in anesthetized adults and to compare its reliability with criteria using changes in heart rate, systolic blood pressure or T-wave amplitude.


Description:

Intravenous injection of local anesthetics could result in life-threatening complications during general anesthesia. Physicians usually use local anesthetics containing epinephrine to detect intravascular injection. Existing methods including heart rate, systolic blood pressure and T-wave amplitude are unreliable to detect intravascular injection during anesthesia and a method using changes in perfusion index was recently suggested. This study was designed to determine whether perfusion index is a reliable method to detect intravascular injection of epinephrine containing local anesthetics and to compare its reliability with conventional criteria in sevoflurane anesthetized adults.

We will randomize patients to 2 groups: a saline group and an epinephrine group. Changes in perfusion index, systolic blood pressure, heart rate and T-wave amplitude will be measured during 5 minutes after injection of 3 mL of saline or 1% lidocaine containing epinephrine. we will determine sensitivity, specificity, positive predictive value and negative predictive value.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date April 2011
Est. primary completion date July 2010
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- ASA physical status 1 patients undergoing general anesthesia for elective surgery

Exclusion Criteria:

- emergent operation

- those who are taking anticoagulant medication, calcium channel blockers, or b-blockers

- laparoscopic operation

- history of smoking

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Drug:
Epinephrine
This group receives 3 mL of 1% lidocaine containing epinephrine IV during operation.
Control
This group receives 3 mL of saline IV during operation.

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary change of perfusion index from baseline we will observe the change of perfusion index from baseline during 5 min after injection of epinephrine containing test dose or saline. Patients whose perfusion index decrease more than 25% are defined as positive response.we will obtain the sensitivity, specificity, positive predictive value, negative predictive value using perfusion index criteria to determine the reliability of perfusion index criteria. during 5 min after injection of epinephrine containing test dose or saline Yes
Secondary change of systolic blood pressure, heart rate, T-wave amplitude from baseline during 5 min after injection of epinephrine containing test dose or saline Yes
See also
  Status Clinical Trial Phase
Completed NCT03145519 - A Trial to Demonstrate the Safety and Efficacy of the OptiVein IV Catheter In a Pediatric Population N/A
Completed NCT03057704 - Comparison of Two Techniques of IV Lidocaine on Propofol Injection Pain Phase 4