To compare two oxygen device during Gastroendoscopy
Phase 4
- Conditions
- Health Condition 1: K299- Gastroduodenitis, unspecified
- Registration Number
- CTRI/2022/12/047907
- Lead Sponsor
- eha Pandey
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients undergoing diagnostic or therapeutic gastrointestinal procedures
2.ASA physical status 1 to 4
3.Patients receiving intravenous sedation for the procedures lasting for more than 30 minutes
Exclusion Criteria
1.History of myocardial infarction and unstable angina pectoris within the past 6 months
2.History of severe arrhythmia
3.Acute pharyngitis, and tonsillitis,pneumonia
4.Pulse oxygen saturation (SpO2) <90% without oxygen inhalation
5.Severe obstructive sleep apnea syndrome
6.Allergy to propofol, eggs, soybean, or albumin
7.Lack of cooperation
8.Pregnancy or lactation
9.Participation in other clinical studies within the previous 3 months. Patients who refused to participate were also excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is defined as any measurement/occurrence of Spo2 â?¤90% during the procedure.Timepoint: Intraprocedural time
- Secondary Outcome Measures
Name Time Method