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UnknownNCT04538820

Dexamethasone Dose for Postoperative Nausea and Vomiting Prophylaxis in Obese Patients

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Diskapi Yildirim Beyazit Education and Research Hospital · Other Government
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

compare the effectiveness of different doses of dexamethasone used for postoperative nausea and vomiting prophylaxis in obese patients and in normal weight patients.

Detailed description

compare the effectiveness of different doses of dexamethasone used for postoperative nausea and vomiting prophylaxis in obese patients. compare the effectiveness of dexamethasone given in 4 mg and 8 mg doses in obese patients with 4 mg doses of dexamethasone in normal weight patients. 4 mg iv dexamethasone will be administered to normal weight patients at induction of anesthesia. This group will be classified as the control group. In obese patients (BMI\>30 kg/m2), one group will receive 4 mg dexamethasone and other group will receive 8 mg dexamethasone at induction. Patients will receive general anesthesia with volatile anesthetics and tramadol will be administered IV at the end of surgery. Postoperative nausea and vomiting, postoperative pain, blood glucose, wound infection, time to oral intake, hospital stay will be compared.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasone 4 mg IV-controldexamethasone 4 mg will be administered at induction of anesthesia for postoperative nausea and vomiting proflaxis to normal weight patients.
DRUGDexamethasone 4 mg IVdexamethasone 4 mg will be administered at induction of anesthesia for postoperative nausea and vomiting proflaxis to obese patients
DRUGDexamethasone 8 mg IVdexamethasone 8 mg will be administered at induction of anesthesia for postoperative nausea and vomiting proflaxis to obese patients

Timeline

Start date
2021-03-01
Primary completion
2021-09-30
Completion
2021-09-30
First posted
2020-09-04
Last updated
2021-09-08

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04538820. Inclusion in this directory is not an endorsement.