Investigation of the use of nasal cannula fixturesQuestionnaire survey of patients regarding the presence or absence of medical device-related pressure injuries, safety, and usability
Not Applicable
- Conditions
- Pneumonia, chronic obstructive pulmonary disease, interstitial pneumonia, respiratory failure, pulmo
- Registration Number
- JPRN-jRCT1030220515
- Lead Sponsor
- Tsuruta Kaori
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
1)Patients who are hospitalized at Showa University Hospital, Showa University Hospital East, or Showa University Koto Toyosu Hospital and have been using a nasal cannula for more than one week.
2) Patients who can be surveyed by questionnaire
3)Patients who have given written informed consent to participate in this study
4)Patients aged 18 years or older at the time of informed consent
Exclusion Criteria
1) Patients with severe mental illness
2) Patients for whom questionnaire survey is impossible
3) Patients judged to be ineligible by the judgment of the research director and co-investigators
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method