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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05860010
Other study ID # MD-375-2020
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 5, 2023
Est. completion date December 5, 2023

Study information

Verified date May 2023
Source Kasr El Aini Hospital
Contact Ayman amin A Abougabal
Phone 1020671408
Email ayman.abougabal@kasralainy.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Electrical cardiometry (EC) is a non-invasive method of estimating cardiac parameters by measuring changes in thoracic bioimpedance during the cardiac cycle. The ICON (Cardiotronic Osypka Medical, San Diego, California) monitor uses four electrocardiogram electrodes and estimates the maximum rate of impedance change to peak aortic blood acceleration. An impedance change occurs between diastole and systole as red blood cell orientation is altered from random during diastole to align during systole. This device is validated against Fick cardiac output and transthoracic echocardiography in infants and children, as well as thermodilution in adults with R values of 0.9. This device is approved by the Food and Drug Administration (FDA) for use in pediatrics. Hypotension is expected to occur after epidural anesthesia (EA) due to the dilatation of venous vessels by sympathetic blockade with a subsequent decrease in venous return and cardiac output (CO). Also, the association of general anesthesia (GA) to EA can lead to more decrease in CO. The addition of epinephrine to local anesthetics (LA) could worsen hypotension through the systemic absorption of epinephrine that leads to a vasodilator β effect. Yet, CO may be enhanced by this β-adrenergic stimulation. However, it is well known that caudal epidural anesthesia has few or no hemodynamic changes in children less than 8 yr old. This could be attributed to the immaturity of their sympathetic system and smaller lower-limbs blood volume compared to adults. Caudal anesthesia is highly effective in abdominal, urinary tract, and lower extremity surgeries in children for intra- and postoperative analgesia. The addition of dexmedetomidine to local anesthetics in caudal anesthesia is a frequent practice. Dexmedetomidine, a highly selective alpha-2 adrenoreceptor agonist, is used as an intravenous sedative and analgesic drug. It has an a2/a1 selectivity ratio of 1600: 1 and is eight times more potent than clonidine. Intrathecal and epidural dexmedetomidine have been reported to produce analgesic properties, prolonging the duration of local anesthetics without causing nerve damage in pediatric patients. Although basal heart rate is greater than in adults, activation of the parasympathetic nervous system, anesthetic overdose, or hypoxia can quickly trigger bradycardia and profound reductions in cardiac output. The sympathetic nervous system and baroreceptor reflexes are not fully mature and the infant cardiovascular system displays a blunted response to exogenous catecholamines. That's why it is very essential to determine the hemodynamic effects of any drug used as an adjuvant to local anesthetics for caudal block and to explore whether it reduces the child cardiac output or not. As invasive cardiac monitors are rarely indicated in pediatric patients, and little is known about the impact of caudally administered dexmedetomidine on cardiac function, so we aimed to investigate its effect on hemodynamic functions measured by EC.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 39
Est. completion date December 5, 2023
Est. primary completion date November 5, 2023
Accepts healthy volunteers No
Gender All
Age group 2 Months to 12 Years
Eligibility Inclusion Criteria: - ASA physical status I and II, pediatric patients aged between 6 months and 8 years, of male or female gender, and undergoing elective infraumbilical (i.e. lower abdominal or genitourinary surgeries) will be included. Exclusion Criteria: - Parent or guardian refusal - Patients < 6 months and > 8 years old - Emergency cases - Surgery lasting > 60 min - Patients with known congenital heart disease. - Patients with history or evidence of infection at the back. - Congenital abnormalities of lower spine or meninges e.g. spina bifida - Patients with blood clotting disorders or on anticoagulation therapy. - Patients with known allergy to systemic or local anesthetics

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Epinephrine injection
patients will be placed on left lateral position and drug will be given the caudal space
Dexmedetomidine
patients will be placed on left lateral position and drug will be given the caudal space
Bupivacaine
patients will be placed on left lateral position and drug will be given the caudal space

Locations

Country Name City State
Egypt Ayman Abougabal [aabougabal] Cairo
Egypt Kasr Al Ainy Cairo

Sponsors (1)

Lead Sponsor Collaborator
Kasr El Aini Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The percentage change in cardiac output after caudal injection the change of cardiac output before and after caudal injection in percent 15 minutes after caudal injection
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