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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04775212
Other study ID # AP2101-50101
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date June 17, 2021
Est. completion date October 17, 2021

Study information

Verified date October 2021
Source National Cancer Institute, Egypt
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It is designed to compare effects of inhaled anaesthetic desflurane and sevoflurane on liver functions in pediatric cancer patients


Description:

Patients will be randomly allocated into two groups using a sealed envelope technique: desflurane group (Des group, n = 30) and sevoflurane group (sevo group, n = 30). Anesthesia monitoring included electrocardiogram, continuous arterial and pulse oximetry, capnography, urine output, nerve stimulator, and esophageal core temperature. Anesthesia will be induced with Propofol 2 mg/kg ,FentanyL 2 μg/kg and atracurium (0.5 mg/kg) was administered to achieve muscle relaxation before endotracheal intubation. End-tidal desflurane or sevoflurane concentrations during the induction were limited to 2 minimal alveolar concentration (MAC). Concentrations of inhalational anesthetics were measured using an anesthetic gas analyser (Datex-Ohmeda, Helsinki, Finland). For the maintenance of anesthesia, the inspired desflurane or sevoflurane concentration was carefully titrated to maintain the end-tidal concentration of 1 MAC. A constant fresh gas flow of 3 l/min (medical-grade air in oxygen to make inspiratory oxygen fraction 0.5) was used during the maintenance of anesthesia. Ventilation was controlled with a tidal volume of 7-10 ml/kg and ventilatory rate was adjusted to maintain an end tidal carbon dioxide ( CO2 )of 35-40 mmHg. to maintain intraoperative blood pressure (BP) and heart rate (HR) within 20% of preoperative values. additional Atracurium will be administered as appropriate. Nerve stimulator was used to monitor neuromuscular blockade on the right adductor pollicis. Hypotension (a drop in systolic BP to the extent of 30% or more or the systolic BP being less than the preoperative values) was treated with volume replacement and, when necessary, with intravenous ephedrine in incremental doses .Bradycardia (HR < 50 beats per min) was treated with atropine if needed. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), total bilirubin (TB), prothrombin time (PT) expressed in international normalized ratio (INR), albumin, platelet count (PLT), and hemoglobin (Hb) were analysed at preoperative period, immediately after operation, and on the 1st, 2nd, 3rd, 5th and 7th, postoperative days (PODs).


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 60
Est. completion date October 17, 2021
Est. primary completion date October 17, 2021
Accepts healthy volunteers No
Gender All
Age group 1 Year to 12 Years
Eligibility Inclusion Criteria: - Age >1 year and < 12 years old. - Estimated time of surgeries within 1-3 hours. - Elevated liver enzymes less than triple folds. Exclusion Criteria: - Patient refusal. - Hepatitis positive patients. - Raising liver enzymes. - Hepatic surgeries.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Des?urane
compare effects of inhaled anaesthetic desflurane and sevoflurane on liver functions.
Sevoflurane
Sevoflurane

Locations

Country Name City State
Egypt National cancer institute Cairo

Sponsors (1)

Lead Sponsor Collaborator
National Cancer Institute, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary liver function test measuring Aspartate aminotransferase (AST) 6 months
Primary ALT measuring alanine aminotransferase (ALT) 6 months
Primary Total bilirubin measuring total bilirubin (TB) 6 months
Primary prothrombin time measuring prothrombin time (PT) expressed in international normalized ratio (INR) 6 months
Primary Albumin measuring level of albumin. 6 months