Health Condition 1: PCS- Health Condition 2: O- Medical and Surgical Health Condition 3: N889- Noninflammatory disorder of cervixuteri, unspecified
Conditions
Interventions
Intervention1: Total inhalational anaesthesia group: Patients will receive total inhalational anaesthesia with O2, N2O and sevoflurane
Control Intervention1: Total intravenous anaesthesia group: Ptien
Sponsors
Amrita Institute of Medical Sciences
Eligibility
Inclusion criteria
Inclusion criteria: Patients of the American Society of Anaesthesiologists (ASA) physical status 1?2, undergoing dilatation and curettage(D and C) procedures as ambulatory day case procedures under general anaesthesia will be included
Exclusion criteria
Exclusion criteria: Patients with known allergy to the drugs used will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the time taken to respond to verbal commands at the end of surgery between 2 groups of patientsTimepoint: 4 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the postoperative nausea and vomiting, surgeon and patient satisfactionTimepoint: At 1 hr post op | — |
Countries
India
Contacts
Public ContactNitu PV
Amrita Institute of medical Sciences
Outcome results
None listed