sefulness of a continuous suction mouthpiece during percutaneous endoscopic gastrostomy: a single-center, prospective, randomized study
Not Applicable
Recruiting
- Conditions
- Patients with brain disease, neurological disease, dementia, temporomandibular joint disorder, disuse syndrome, or a psychiatric disorder who were scheduled to undergo PEG or the exchange of a gastrostomy button or tube with endoscopy
- Registration Number
- JPRN-UMIN000008575
- Lead Sponsor
- akaya Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Patients had a history of respiratory problems that could increase the risk of complications .
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method