Health Condition 1: null- undergoing laparoscopic cholecystectomy
Conditions
Interventions
Intervention1: 5% dextrose group: Patients received one litre of 5% dextrose after surgery in the recovery room over a period of 30-40 min.
Control Intervention1: Ringer Lactate (RL)group: Patients r
Sponsors
Postgraduate Institute of medical Education and Research
Eligibility
Inclusion criteria
Inclusion criteria: 120 patients of ASA physical status I and II of both genders aged between 19 -60 yrs undergoing LC were included in the study.
Exclusion criteria
Exclusion criteria: 1. Diabetes mellitus, significant cardiac, hepatic or renal disease 2. GIT disease 3. Laparoscopy replaced by laparotomy 4. Previous history of PONV/ motion sickness 5. Patients with body mass index (BMI) >30 kg/m2 6. Currently receiving steroids or antiemetics 7. Allergy to study drugs. 8. Pregnancy or menstruation 9. Patients who cannot be contacted by telephone. 10. Abnormal blood glucose on morning of surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| incidence of nausea and vomitingTimepoint: 0minutes, 30 minutes, 2 hours and 6 hours postoperatively | — |
Secondary
| Measure | Time frame |
|---|---|
| Requirement of rescue antiemetic therapy, postoperative pain, state of well being and length of stay in PACU were also evaluated as secondary objectives.Timepoint: 0-6 hours,6-24 hours postoperatively | — |
Countries
India
Contacts
Public ContactDr Divya Jain
Postgraduate Institute of medical Education and research
Outcome results
None listed