Acute abdomen, Acute appendicitis
Conditions
Interventions
All participants will receive the same anesthetic technique except for the medications that will characterize the group of their participation. All participants will receive 100% oxygen, venous access
Drug
D08.811.277.040.025.095
Sponsors
Centro Universitário Tiradentes
Centro Universitário Tiradentes
Eligibility
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Patient diagnosed with acute appendicitis; Physical status ASA I and II; Age between 18 and 70 years.
Exclusion criteria
Exclusion criteria: Pregnancy; Neuromuscular disease; renal insufficiency; Body mass index greater than 30 km.m-2; Anticipation of difficulty in handling the airway; Chronic use of calcium channel blockers; Chronic use of medicines containing magnesium; Past allergy to magnesium sulfate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical condition of tracheal intubation. It will be verified by means of laryngoscopy, positioning of the vocal cords and reactions that the patient presents at the moment of passage of the orotracheal tube in the airways. It will be evaluated using the intubation score system of the Good Clinical Research Practice guidelines. It will be classified as an acceptable and unacceptable clinical condition. Unacceptable clinical condition will occur if laryngoscopy is difficult, vocal cords are closed, or if there is muscle reaction at the time of passage of the tube through the vocal cords. Classification is by visual inspection. | — |
Secondary
| Measure | Time frame |
|---|---|
| Heart rate, systemic blood pressure, adverse events and oxygen saturation. The heart rate will be verified by pulse oximetry and will be considered alteration when there is an increase or decrease of 10% of the initial value. Systemic blood pressure will be assessed using the sphygmomanometer. It is measured in mmHg and will be considered change when there is an increase or decrease of 10% of the initial value. The net research adverse events will be nausea, vomiting, hyperemia, arrhythmias and sweating. It will be collected through clinical observation. The arterial oxygen saturation will be collected by means of pulse oximetry and its value is shown in percentage number. | — |
Countries
Brazil
Contacts
Public ContactFabiano Barbosa
Centro Universitário Tiradentes
Outcome results
None listed