general surgery.
Conditions
Interventions
Intervention 1: Intervention group: After anesthesia induction with propofol (B.BRAUN ) at an induction dose of 2–2.5 mg/kg (based on body weight), and when the surgery is completed, patients will be
Sponsors
Babol University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age 18 years and older candidate for general anesthesia with endotracheal intubation being in a high-risk cardiovascular or respiratory patient group
Exclusion criteria
Exclusion criteria: Patients with severe tracheal stenosis active respiratory tract infection known airway obstruction emergency surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| O2 saturation. Timepoint: Pre-, intra-, and post-extubation. Method of measurement: Pulls Oximetry. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: Immediately after extubation and at 5, 10, 15, 20, 25 and 30 minutes thereafter. Method of measurement: Cardiac monitoring.;Heart rate. Timepoint: Immediately after extubation and at 5, 10, 15, 20, 25 and 30 minutes thereafter. Method of measurement: Cardiac monitoring.;Arrhythmia. Timepoint: Immediately after extubation and at 5, 10, 15, 20, 25 and 30 minutes thereafter. Method of measurement: Cardiac monitoring.;Cough. Timepoint: After extubation. Method of measurement: Report writing sheet.;Bronchospasm. Timepoint: After extubation. Method of measurement: Report writing sheet. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contacthasanali jafarpoor
Babol University of Medical Sciences
Outcome results
None listed