to study the effect of Metocloparamide and Dexamethsone drugs in reducing vomiting in patients undergoing laproscopic cholecystectomy
Not Applicable
- Conditions
- Health Condition 1: null- patients of ASA grade I&II planned for laproscopic cholycestectomypatients age of 18-55yrpatients weight between 30-75kg
- Registration Number
- CTRI/2012/05/002668
- Lead Sponsor
- Subharti Medical College Meerut
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
pt. of ASA grade I & II ,
weight between 30 to 75kg
Exclusion Criteria
Pt ASA grade 3 & 4
Pt who have received opoids ,steroids and any antiemetic within 24hr
Pt having contraindication or hypersensivity to metocloparamide
pregnant female
Pt having history of PONV & motion sickness
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) To evaluate the efficacy of i.v dexamethasone 5mg + metocloparamide 10mg on PONV <br/ ><br>2) To evaluate the efficacy of i.v dexamethasone 2.5mg + metocloparamide 10mg on PONV <br/ ><br>3)To evaluate the efficacy of i.v metocloparamide 10mg on PONVTimepoint: at 0-1hr <br/ ><br>at 1-4 hr <br/ ><br>at 4-8hr <br/ ><br>at 8-12hr <br/ ><br>at 12-24hr
- Secondary Outcome Measures
Name Time Method comperative evaluation of these drug on POnVTimepoint: at 0-1hr <br/ ><br>at 1-4 hr <br/ ><br>at 4-8hr <br/ ><br>at 8-12hr