Comparison of the Effects of Neostigmine With Sugammadex on Postoperative Nausea and Vomiting.
- Conditions
- Incidence of Postoperative Nausea and Vomiting
- Interventions
- Registration Number
- NCT02286752
- Lead Sponsor
- T.C. ORDU ÜNİVERSİTESİ
- Brief Summary
Postoperative nausea and vomiting is one of most common complications after general anesthesia. Female sex, history of postoperative nausea and vomiting, motion sickness, non smoker status, opioid administration are known as risk factors for developing postoperative nausea and vomiting.
It has been suggest that antagonism of residual neuromuscular block with a mixture of neostigmine and atropine at the end of the surgery increases the risk of postoperative nausea and vomiting.
Sugammadex is a very safe drug with almost no serious adverse effects. The known adverse effects include slight coughing, movement, an altered taste sensation in the mouth, transient prolongation of the QT interval, hypersensitivity, and a short term prolongation of the activated partial thromboplastin time.
The aim of this study was to compare the sugammadex versus neostigmine plus atropine for reversal of rocuronium induced neuromuscular blockade in terms of incidence of postoperative nausea and vomiting.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 98
- American Society of Anesthesiologists (ASA) physical status 1 and 2
- endotracheal intubation and general anesthesia scheduled for elective surgery
- age < 18 years, > 65 years
- pregnancy
- refusal to participate and patients already participating in another study
- allergy to study drugs
- communication difficulty
- psychiatric and neurological disorders
- use of analgesics or sedative or antiemetic drugs within 24 hours before surgery.
- emergency surgery
- history of drug or alcohol abuse
- ASA 3 and above
- patients with vertigo
- Laparoscopic surgery, oncologic surgery, strabismus and mid ear surgery neurosurgery, gynecologic surgery, breast surgery
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description neostigmine Neostigmine - sugammadex sugammadex -
- Primary Outcome Measures
Name Time Method Verbal Descriptive Scale within postoperative 24 hours 0: no nausea 1: mild 2: moderate 3: severe
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Anesthesiology and Reanimation Dept. Ordu University Training and Research Hospital
🇹🇷Altınordu, Ordu, Turkey