Comparitive study of two antiemetic drugs group to decrease the chances of emesis after Laproscopic Cholecyestectomy
- Conditions
- Health Condition 1: null- SYMPTOMATIC CHOLILITHIASIS FOR LAPROSCOPIC SURGERIES
- Registration Number
- CTRI/2018/07/014830
- Lead Sponsor
- Dr RPGMC TANDA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 84
Patients in the age group of 20-60 years.
1.ASA I â??II
2.Patient willing to give consent for study.
3.No history of motion sickness.
4.No previous history of PONV.
5.Nonsmoker.
1.Patients not giving consent for study.
2.Patients with history of taking drugs responsible for antiemetic action for eg. steroids etc.
3.Smoker.
4.Patient with gastrointestinal reflux diseases.
5.Patient with history of PONV or motion sickness and those who had allergy to the study drugs or received antiemetic within 48 h before surgery.
6.Pregnancy and lactation.
7. Body mass index >35 kg/m2.
8.Patients with Baseline prolonged QTc interval.
9. Patients with electrolyte imbalances.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method