Health Condition 1: null- healthy or mild functional limitation
Conditions
Interventions
Intervention1: Group II(Valsalva)
: Group II(Valsalva) Patients were asked to blow into a rubber tubing connected to sphygmomanometer and raise the mercury column up to 30 mmHg for a period of a
Sponsors
Sanjay Gandhi Postgraduate Institute Of Medical Sciences Lucknow Uttar Pradesh India
Eligibility
Inclusion criteria
Inclusion criteria: ASA I patients scheduled for surgery under general anaesthesia with propofol as an induction agent
Exclusion criteria
Exclusion criteria: Patient refusal Patients with communication problem Cardiorespiratory disease Chronic pain disorder, on preoperative analgesic medication, History of egg allergy, soyabean oil Inability to perform valsalva
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the analgesic efficacy of valsalva procedure in attenuating the propofol pain at induction of general anaesthesiaTimepoint: 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| nilTimepoint: N/A | — |
Countries
India
Contacts
Public ContactSanjay kumar
Sanjay Gandhi Post Graduate Institute of Medical Sciences
Outcome results
None listed