Viewing Study NCT04538820


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Ignite Modification Date: 2025-12-26 @ 3:20 AM
Study NCT ID: NCT04538820
Status: UNKNOWN
Last Update Posted: 2021-09-08
First Post: 2020-08-13
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Dexamethasone Dose for Postoperative Nausea and Vomiting Prophylaxis in Obese Patients
Sponsor: Diskapi Yildirim Beyazit Education and Research Hospital
Organization:

Study Overview

Official Title: Dexamethasone Dose for Postoperative Nausea and Vomiting Prophylaxis in Obese Patients
Status: UNKNOWN
Status Verified Date: 2021-09
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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.

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: