Hypotention induced by spinal anesthesia.
Conditions
Interventions
Intervention 1: Intervention group: Patients are among the candidates for orthopedic surgery for spinal anesthesia who have no contraindications to spinal anesthesia and have been fasting for at least
Sponsors
Jahrom University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Candidates for orthopedic surgery by spinal anesthesia at Peymanieh Hospital in Jahrom Satisfaction of the person to participate in the study age between 18 to 65 years
Exclusion criteria
Exclusion criteria: Patients with hypertension weight more than 100 kg motion sickness cardiac and liver desease and migrain allery to ondansetron drugs using any drugs that change blood pressure or hear rate and any drugs that effects by serotonin receptor
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of people with hypotension. Timepoint: Blood pressure measurement during the first 10 minutes, every 3 minutes and then every 5 minutes until the end of 30 minutes of spinal anesthesia. Method of measurement: Measurement with heart monitoring device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Percentage of people with decreased heart rate. Timepoint: during the first 10 minutes, every 3 minutes and then every 5 minutes until the end of 30 minutes of spinal anesthesia. Method of measurement: Measuring heart rate with a heart rate monitor.;Percentage of people with pruritus after spinal anesthesia. Timepoint: Every 10 minutes after spinal anesthesia. Method of measurement: by asking the patient.;Percentage of people with nausea after spinal anesthesia. Timepoint: Every 10 minutes after spinal anesthesia. Method of measurement: by asking the patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNasim Nabizadeh
Jahrom University of Medical Sciences
Outcome results
None listed