A clinical trial to study the effect of perioperative dextrose solution on postoperative nausea and vomiting
- Conditions
- Health Condition 1: K801- Calculus of gallbladder with othercholecystitisHealth Condition 2: C509- Malignant neoplasm of breast of unspecified siteHealth Condition 3: H679- Otitis media in diseases classified elsewhere, unspecified ear
- Registration Number
- CTRI/2019/08/020944
- Lead Sponsor
- Department of Anaesthesiology and critical Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Patients undergoing elective laparoscopic cholecystectomy ear nose throat surgery and breast surgery requiring general anaesthesia
Patients who are nonsmokers
Patients comming under American Society of Anesthesiologists Physical Status I and II
Patients refusal
Pregnant women and lactating mothers
Patients with history of coronary artery disease congestive heart failure Diabetes mellitus Renal insufficiency Gastro esophageal reflux disease and patients receiving antiemetic and steroid medication
Abnormal blood glucose on the morning of surgery fasting blood glucose more than 140 mg per dL
Patient with increased intracranial tension due to some pathology eg Intracranial space occupying lesion ICSOL meningitis Pseudotumourcerebri
Patient unable to give informed consent
Patients with BMI more than or equal to 35
Patients will be excluded from analysis if,they require large volume of intravascular fluid treatment for severe intraoperative hypotension or if the surgery progressed to additional procedures or the patient needed a repeat surgical intervention radiological intervention with contrast or anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method