patient who underwent endoscopic ultrasonography Recovery time,
Conditions
Interventions
Patients were pharyngeal topicalized with normal saline (Group N),Patients were pharyngeal topicalized with lidocaine spray (Group L)
Placebo Comparator Drug,Active Comparator Drug
Group N,Gruop L
Sponsors
Naruenart Lomarat
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: . Patients with American Society of Anesthesiologists (ASA) physical status class I-III, age between 18 and 65 years who presented for EUS procedures were eligible for the study
Exclusion criteria
Exclusion criteria: patients with severe cardiorespiratory instabilities, severe hypertension, psychological abnormality, end staged renal disease, any clinical evidence of hepatic encephalopathy, pregnancy, and refusal to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| recovery time after the end of intervention to awakening time postanesthetic recovery score/ discharge score | — |
Secondary
| Measure | Time frame |
|---|---|
| complications related propofol-based deep sedation after the end of intervention awakening time count of complication related events | — |
Countries
Thailand
Contacts
Public Contactnaruenart lomarat
Department of Anesthesiology, Faculty of medicine, Siriraj Hospital, mahidol University
Outcome results
None listed