Evaluation of the effects of hydrocortisone on hemodynamic changes in patients under general anesthesia
Phase 3
Recruiting
- Conditions
- Patients for elective surgery for upper limb fractures.Fracture of upper limb, level unspecified
- Registration Number
- IRCT20170108031818N2
- Lead Sponsor
- Gorgan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 48
Inclusion Criteria
All patients for elective surgery between the ages of 15-60 with ASA I or II
Exclusion Criteria
All patients for elective surgery between the ages of 15-60 with ASA I or II
Metabolic and neuromuscular disorders
People if they receive strong antibiotics effective on the effects of relaxants, including aminoglycosides 24 hours before surgery
Significant liver and kidney disease
Known allergies to narcotics and other drugs used during anesthesia
if he took the H1 histamine blocker the day before surgery
Obesity (if ideal body weight> 30)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hemodynamic changes. Timepoint: Hemodynamics will be recorded in the relevant list before the administration of hydrocortisone and 30 minutes after the administration of hydrocortisone or at the entrance to the operating room and 5 minutes after the peak effect of atracurium (before intubation) and after ecstasy. Method of measurement: This monitoring will be performed under the supervision of an anesthesiologist based on patient monitoring instructions, including continuous monitoring of heart rate, arterial oxygen saturation and intermittent and non-invasive measurement of systolic and diastolic blood pressure and bronchospasm by Saadat's monitoring device.
- Secondary Outcome Measures
Name Time Method