Health Condition 1: - Health Condition 2: 4- Measurement and Monitoring
Conditions
Interventions
Intervention1: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
Nil
Eligibility
Inclusion criteria
Inclusion criteria: Patients with a recorded time of last clear fluid intake on the day of surgery. ASA physical status I & II
Exclusion criteria
Exclusion criteria: 1. ASA PS III and above 2. Preoperative heart rate less than 45 beats/minute 3. Preoperative mean arterial blood pressure less than 65 mmHg 4. Obesity with BMI more than 30 5. Height less than 150 cm and more than 180 cm 6. Weight less than 50 kg and more than 80 kg 7. Patients with cardiac arrhythmia, or on rate/vascular tone modulation therapy 8. Patients who received intravenous fluid administration during the preanaesthesia fasting period 9. Pregnant women and lactating mothers 10. Patients unwilling to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine the preoperative fasting duration specific effect on incidences of low systolic blood pressure in the early phase (0-5 min) and secondary phase (6-30 min) after Spinal anaesthesia induction.Timepoint: Early phase (0-5 min) Secondary phase (6-30 min) | — |
Secondary
| Measure | Time frame |
|---|---|
| To determine the association between clear fluids fasting duration and the incidence of low blood pressure To observe any association between clear fluids fasting duration and occurrence of Nausea, vomiting, shivering, discomfort, allergic reaction, or any other complications Timepoint: Initial 5 to 30 mins | — |
Countries
India
Contacts
Public ContactDr Aloka Samantaray
Sri Venkateswara Institute of medical sciences(SVIMS)
Outcome results
None listed