The Impact of Comprehensive Education Before Gastroscopy on Improving the Tolerance of Patients
- Conditions
- Comprehensive Education
- Registration Number
- NCT03638752
- Lead Sponsor
- Ningbo No. 1 Hospital
- Brief Summary
This clinical trial is being conducted to assess whether the comprehensive education before gastroscopy could reduce the adverse reactions, such as nausea, vomiting and improve patient satisfaction.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 260
- Patients over the age of 18 years undergoing routine gastroscopy
- Informed consent
- Serious coronary heart disease and myocardial injury with serious heart failure
- Stenosis of the esophagus or cardia obstruction
- Acute pharyngitis and tonsillitis
- Acute upper gastrointestinal bleeding
- Hemodynamically unstable
- allergy to topical lidocaine
- Patients did not cooperate or spirit was not normal
- Pregnancy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Adverse reaction times in gastroscopy 1 day research assistant records nausea/vomiting/retching times in the whole process of gastroscopy
- Secondary Outcome Measures
Name Time Method Patients' tolerance scores 1 day At the end of the procedure, the patients were asked about the tolerance in the process of gastroscopy by using a 100-mm visual analogue scale. Tolerance includes the extent of pain and nausea. The endpoints were assigned "no nausea or no pain " to the left and "worst possible nausea or worst pain imaginable " to the right.
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Trial Locations
- Locations (1)
Ningbo NO.1 hospital
🇨🇳Ningbo, Zhejiang, China
Ningbo NO.1 hospital🇨🇳Ningbo, Zhejiang, China