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Etco2 Levels on the End-tidal Concentration of Sevoflurane

T

Tanta University

Status

Completed

Conditions

Minimum Alveolar Concentration
End-tidal Sevoflurane
End-tidal Carbon Dioxide

Treatments

Procedure: high etco2
Procedure: normal etco2
Procedure: low etco2

Study type

Interventional

Funder types

Other

Identifiers

NCT05778968
MAC of sevoflurane

Details and patient eligibility

About

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

Full 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.

Enrollment

90 patients

Sex

All

Ages

30 to 65 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

90 participants in 3 patient groups

low ETCO2
Active Comparator group
Treatment:
Procedure: low etco2
normal ETCO2
Active Comparator group
Treatment:
Procedure: normal etco2
high ETCO2
Active Comparator group
Treatment:
Procedure: high etco2

Trial contacts and locations

1

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Central trial contact

tarek A Mostafa, MD

Data sourced from clinicaltrials.gov

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