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Comparitive study of two antiemetic drugs group to decrease the chances of emesis after Laproscopic Cholecyestectomy

Not Applicable
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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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