Construction and Effectiveness Evaluation of Painless Digestive Endoscopy Mode Led by Anesthesia Nurses Under the Guidance of Anesthesiologists
NCT ID: NCT06712264
Last Updated: 2025-11-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
18000 participants
OBSERVATIONAL
2024-12-01
2025-02-28
Brief Summary
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Detailed Description
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The main problem causing this situation is the severe shortage of anesthesiologists in China at present. The current number of anesthesiologists in China is 100000, with a shortage of up to 250000 anesthesiologists. The existing number of anesthesiologists is already struggling to cope with the annual surgical workload of nearly 60 million researchers. Long term high workload and high pressure have led to a constant occurrence of overwork and death among anesthesiologists. Anesthesiology is the department with the highest sudden death rate among all clinical departments.
In this context, researchers creatively proposed and implemented a painless diagnosis and treatment model led by anesthesia nurses under the guidance of anesthesiologists in 2019, which improved work efficiency and economic resource utilization, saved medical costs, met the people's demand for comfortable diagnosis and treatment, and effectively solved the problem of shortage of anesthesiologists. However, there is still a lack of unified standards for the training, assessment, admission, supervision, and diagnosis and treatment processes of anesthesia nurses involved in the effective operation of this model, and its effectiveness and safety also lack convincing evidence.
2. Research objective Verify the effectiveness and safety of the painless digestive endoscopy mode led by anesthesia nurses under the guidance of anesthesiologists.
3. Research significance Through this study, we will further standardize the training, assessment, admission, supervision, and diagnosis and treatment processes for anesthesia nurses, and verify the effectiveness and safety of this model through quality evaluation tools and indicators such as doctor-patient satisfaction. This will provide a basis for the further promotion of this model and open up a new path for the effective development of comfortable medical safety.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Exposed Group
Sedation administered by anesthetic nurses under the guidance of anesthesiologists
No interventions assigned to this group
Unexposed Group
Sedation administered by anesthesiologists
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* no oral intake before surgery: liquid for 2 hours, solid for 6 hours.
Exclusion Criteria
* sleep apnea,
* allergies to soybeans, eggs, or peanuts,
* pregnancy,
* previous anesthesia related complications,,
* potential difficult ventilation,
* acute gastrointestinal bleeding,
* sub intestinal obstruction,
* severe chronic obstructive pulmonary disease (COPD)
16 Years
ALL
No
Sponsors
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The Affiliated Hospital of Qingdao University
OTHER
Responsible Party
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jixiangyu
Principal Investigator
Locations
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the Affiliated Hospital of Qingdao University
Qingdao, Shandong, China
Countries
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Other Identifiers
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QYFYEC2024-234
Identifier Type: -
Identifier Source: org_study_id
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