Propofo-Based deep sedation for endoscopic ultrasography

Not Applicable

Completed

• Conditions: patient who underwent endoscopic ultrasonography; Recovery time, Complication, Deep sedation, Propofol, Endoscopic Ultrasonography, Topical pharyngeal anesthesia

• Registration Number: TCTR20170526001
• Lead Sponsor: aruenart Lomarat

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2016-03-11
• Study Start: 2017-05-26
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 32

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

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
recovery time after the end of intervention to awakening time postanesthetic recovery score/ discharge score

Secondary Outcome Measures

Name	Time	Method
complications related propofol-based deep sedation after the end of intervention awakening time count of complication related events