ClinicalTrials.Veeva

Menu

The Effect of Anesthetic Agents Management on ECG Changes of Patients Who Were Operated Under RIVA

D

Duzce University

Status

Completed

Conditions

Qt Interval, Variation in

Treatments

Drug: Ketamine HCL

Study type

Interventional

Funder types

Other

Identifiers

NCT02063620
gokceakman
ilknurseker (Other Identifier)

Details and patient eligibility

About

IVRA can be performed with many local anesthetics and adjuvant agents. Investigators planned to compare cardiac effects and ECG changes by IVRA with lidocaine and lidocaine plus ketamine.

Full description

Methods: Patients between 18-60 years, with score of ASA 1-2 and who were undergoing IVRA for short operations on arm and forearm were included. Systolic, diastolic and mean blood pressures, heart rate, SpO2, ECG, adverse effects during the operation were recorded. Double cuffed tourniquet were placed on the extremity to be operated to hinder nerve injuries. Venous blood in the extremity was purged with Esmarch bandage. Proximal cuff was inflated with a pressure 50-100 mmHg higher than systolic blood pressure and the bandage was displaced. Randomly patients were divided into 2 groups. Group 1: %0.5 Lidocaine+Ketamine 0.8 mg/kg; 40 ml. Group 2: %0.5 Lidocaine 40 ml. Anesthetic agent was injected with a rate of 20 ml/min. 20 minutes after injection the distal cuff was inflated and the proximal cuff deflated with a rate of 50 mmHg in every 3 minutes. 0,5,10,15,30,45,60 minutes after the beginning of deflation and 10 minutes after the deflation was completed ECG were recorded. PR,QT,QTc, RR were recorded.

Enrollment

60 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Patients between 18-60 years
  2. ASA 1-2 physical status
  3. Undergoing IVRA for short operations on arm and forearm

Exclusion criteria

  1. Allergy to study drugs,
  2. Serious cardiac diseases,
  3. Respiratory diseases,
  4. Renal failure,
  5. Drug addiction,
  6. Pregnancy,
  7. Liver failure,
  8. Hypertension,
  9. Genetic diseases of musculoskeletal system,
  10. Use of antiepileptic drugs, abnormal thyroid functions and operation period over 1 hour.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

60 participants in 2 patient groups

ketamine HCL
Active Comparator group
Description:
%0.5 Lidocaine+Ketamine HCL 0.8 mg/kg, total 40ml, single dose administration, 30 minute duration, total 200mg lidocaine
Treatment:
Drug: Ketamine HCL
lidocaine+ serum physiologic
No Intervention group
Description:
% 0.5 lidocaine+ serum physiologic, total 40ml, total 200 mg lidocaine, 30 minute duration, single dose administration,

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems