Health Condition 1: C509- Malignant neoplasm of breast of unspecified site Health Condition 2: null- Patients scheduled for elective surgery of age 18yrs with breast cancer, ASA grade 1-3
Conditions
Interventions
Intervention1: Aprepitant: Patients in group I will receive 80 mg oral Aprepitant 3 hours before induction of anesthesia
Control Intervention1: Dexamethasone: Patients in group II will receive 8mg dex
Sponsors
AIIMS
Eligibility
Inclusion criteria
Inclusion criteria: Patients scheduled for elective surgery of age >18yrs with breast cancer, ASA grade 1-3
Exclusion criteria
Exclusion criteria: patients who had a history of drug abuse, hypersensitivity reaction, nausea and received antiemetic before surgery within 24 hours, pregnancy, breastfeeding status
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary efficacy variable will be episodes of nausea and or vomiting in the early and late postoperative period in first 24 hoursTimepoint: The primary efficacy variable will be episodes of nausea and or vomiting in the early and late postoperative period in first 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| The incidence of any adverse reaction to treatment in the two experimental groups will be recordedTimepoint: till discharge | — |
Countries
India
Contacts
Public ContactSACHIDANAND JEE BHARATI
ALL INDIA INSTITUTE OF MEDICAL SCIENCES
Outcome results
None listed