difference in postoperative nausea and vomiting after ondansetron and granisetron in patient with hysterectomies
Not Applicable
Completed
- Conditions
- Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecified
- Registration Number
- CTRI/2019/03/018150
- Lead Sponsor
- SDMH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 160
Inclusion Criteria
1.Females of ASA grade I and II
2.Females of age 18-55 yrs
3.Patient who gives informed written consent
4.Females who are undergoing laproscopic hysterectomies
Exclusion Criteria
ASA � grade III
2. Females with major systemic illness
3. Patient with history of PONV in previous surgery
4. Patient with history of vomiting and ryleââ?¬•s tube in situ in last 24 hours
5. Patient with history of allergy to the drug
6. Patient who refuse to give consent
7. Patient having neurological and renal diseases.
8. Pregnant females
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method incidence of post operative nausea and vomitingTimepoint: for 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method assess demand of rescue antiemetic. <br/ ><br>compare side effects of ondansetron and granisetronTimepoint: intraoperatively and for 24 hours post operatively