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comparison of 3 medicine and 2 medicines for prevention of vomiting after surgery.

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/01/049005
Lead Sponsor
AIIMS
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

FEMALE >18 YRS,NON SMOKERS UNDERGOING LAPAROSCOPIC SURGERY LASTING 2-4 HOURS, RECEIVING INTRAOPERATIVE AND POSTOPERATIVE OPIOID ANALGESIA.

Exclusion Criteria

1. CONSUMPTION OF AN AGENT WITH ANTI EMETIC PROPERTIES WITHIN 24 HRS PRIOR TO COMMENCEMENT OF THE STUDY.

2. KNOWN HYPERSENSITIVITY TO APREPITANT, ONDANSETRON OR DEXAMETHASONE.

3. PREGNANCY.

4. PATIENTS REQUIRING POSTOPERATIVE MECHANICAL VENTILATION.

5. SURGERY LASTING >4 HRS

6. TIVA

7. PATIENTS NOT GIVING CONSENT.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
TO COMPARE THE INCIDENCE OF POSTOPERATIVE NAUSEA AND VOMITING.Timepoint: 2 HOURS AND 24 HOURS FOLLOWING SURGERY.
Secondary Outcome Measures
NameTimeMethod
TIME TO FIRST RESCUE ANTIEMETIC AND THE AMOUNT OF ANTIEMETIC CONSUMED.Timepoint: FIRST 24 HOURS.
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