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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05778968
Other study ID # MAC of sevoflurane
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 1, 2023
Est. completion date August 2024

Study information

Verified date April 2024
Source Tanta University
Contact tarek A Mostafa, MD
Phone +20403288260
Email dr.tarek311@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

he assessment of adequate levels of anaesthesia traditionally relies not only on a patient's movement but also on the hemodynamic response (or both) to a surgical stimulus


Description:

Currently a derivative of MAC namely, end tidal partial pressure (FET) displayed on the work station as concentration , maybe an alternative useful measure of the anaesthetic effect of an inhaled anaesthetic agent . Many pharmacological factors have been associated with alterations in MAC and Mac derivatives such as nonsteroidal anti-inflammatory drugs (NSAIDs), analgesics, and anesthetics. However, few studies have focused on physiological factors, such as hypercarbia or hypocarbia. A correlation has been found between Paco2 and Etco2 in ventilated patients with healthy lungs. Some authors have suggested that Etco2 could be considered appropriate for estimating Paco2 even in critical patients. Knowledge of the effects of Paco2 on end tidal concentration of sevoflurane among patients undergoing laparoscopic cholecystectomy may help anaesthesiologists titrate sevoflurane carefully and precisely during different mechanical ventilation settings to avoid dose-dependent hypotension, impaired cardiac contractility, and hypothermia caused by excessive anaesthetic depth of sevoflurane.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date August 2024
Est. primary completion date June 1, 2024
Accepts healthy volunteers No
Gender All
Age group 30 Years to 65 Years
Eligibility Inclusion Criteria: - American Society of anaesthesiologist ASA physical status I, II - admitted for laparoscopic cholecystectomy Exclusion Criteria: - Refusal of patients. - Patients with renal or liver dysfunction. - Patients with chronic pain other than cholelithiasis. - Cardiac disorders as uncontrolled hypertension, arrhythmia, Ischaemic heart disease, valvular heart disease and pulmonary hypertension. - Patient with haematological disorder as Sickle cell disease. - Chest patient as asthma, COPD. - Combined surgery . - History of allergy to any of the study drugs. - Patients with communication problems, cognitive dysfunction, or psychological disorders. - Patients who received analgesics or sedatives 24 h before a scheduled surgery. - Alcohol or drug abuse.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
low etco2
Etco2 levels will be adjusted at levels ranging between 25 mm Hg and 30 mm Hg
normal etco2
Etco2 levels will be adjusted at levels ranging between 31 mm Hg and 40 mm Hg
high etco2
Etco2 levels will be adjusted at levels ranging between 41 mm Hg and 45 mm Hg

Locations

Country Name City State
Egypt tarek Abdelhay Mostafa Tanta El Gharbyia

Sponsors (1)

Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary end tidal concentration of sevoflurane end tidal concentration of sevoflurane is measured by multiple gas analyser during operation Total time of operation
See also
  Status Clinical Trial Phase
Completed NCT04281589 - End-tidal Carbon Dioxide Monitoring in Low Tidal Volume Ventilation N/A
Completed NCT05746949 - Comparison of the Effects of High-flow Nasal Cannula Oxygen and Jet Ventilation Techniques N/A