Ankara University
Ankara, 06550, Turkey (Türkiye)
NCT Number: NCT02026999
The purpose of this study to determine the effectiveness of sugammadex in septoplasty patients whose mask ventilation would be difficult after extubation.
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Notify Me18 year–65 year
All sexes
Observational
Ankara, 06550, Turkey (Türkiye)
Patients undergoing septoplasty operation will be included to this study. After coming to operation room all the patients will have standard monitorisation and induction. After intubation they will have inhalational anesthesia as maintenance. According to the TOF (train of four) measurement all patient will have neuromuscular relaxant if needed. After the operation they will be extubated according to TOF or clinical parameters. And time for extubation, mask assistance need, any complication, mask difficulty, and time spent in postoperative care unit will be recorded. Then the results will be compared, whether sugammadex or neostigmine is better for these patients in means of extubation and postoperative status.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
ASA (American Society of Anesthesiologist) I-II patients undergoing septoplasty operation
Exclusion criteria
Time frame: time between end of surgery and extubation of the patient, approximately 5 to 10 minutes
Time frame: time spent in postanesthesia care unit approximately 10 to 60 minutes
Ankara University
Other
Phase IV Study of the Use of Sugammadex Versus Neostigmine in Septoplasty Operations
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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