Testing of the Apnea Prevention Device
Phase 1
Completed
- Conditions
- Respiratory DepressionElective Surgery
- Interventions
- Other: Verbal promptOther: Skin Stimulus
- Registration Number
- NCT00875134
- Lead Sponsor
- Oregon Health and Science University
- Brief Summary
This study is designed to test the ability of a computer-based algorithm to detect and intervene in cases of narcotic-induced respiratory depression.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
- Elective surgical patients
Exclusion Criteria
- Refusal to consent to study
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Verbal prompt, cutaneous stimulation Skin Stimulus Patient receives either or both a verbal stimulus or cutaneous stimulus Verbal prompt, cutaneous stimulation Verbal prompt Patient receives either or both a verbal stimulus or cutaneous stimulus
- Primary Outcome Measures
Name Time Method Efficacy in treating respiratory depression seconds after desaturation
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Oregon Health and Science University
🇺🇸Portland, Oregon, United States