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NCT03736824 Clinical Trial

Correlation of Endoscopic Findings and Symptoms in Patients Undergoing the First Upper Gastrointestinal Endoscopy

Malignancy Clinical Trial

Official title:
Correlation of Endoscopic Findings and Symptoms in Patients Undergoing the First Upper Gastrointestinal Endoscopy

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03736824
Other study ID # rjyy20181021
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date December 31, 2018

Study information
Verified date November 2018
Source Shanghai Jiao Tong University School of Medicine
Contact Huiyi Li
Phone +8613761902402
Email lhy177279@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Endoscopy is the best means of finding early stage of upper gastrointestinal diseases, especially early cancer and benign ulcers. Currently, most people still undergo upper gastrointestinal endoscopy due to discomfort, rather than a regular physical examination at a certain age. This study prospectively investigated the reason for undergoing the first upper gastrointestinal endoscopy in patients and found the correlation of endoscopic findings and symptoms.

Recruitment information / eligibility
Status Recruiting
Enrollment 5000
Est. completion date December 31, 2018
Est. primary completion date November 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients undergoing the first upper gastrointestinal endoscopy.

Exclusion Criteria:

- The patients had previously performed endoscopy and any esophageal, gastric or duodenal surgery.

- The patients couldn't complete the questionnaire survey under the guidance of physicians at the appointment of the upper gastrointestinal endoscopy.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• endoscopy
All endoscopy was performed by qualified gastroenterologists or endoscopic physicians in Renji hospital,Shanghai Jiaotong University School of Medicine.

Locations
Country Name City State
China Renji Hospital, Shanghai Jiaotong University School of Medicine Shanghai

Sponsors (1)
Lead Sponsor Collaborator
Shanghai Jiao Tong University School of Medicine

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Correlation of endoscopic findings and symptoms survey Within two weeks after receiving the survey
Secondary The proportion of various symptoms in patients undergoing the first upper gastrointestinal endoscopy Within two weeks after receiving the survey
Secondary The proportion of different upper gastrointestinal diseases Diagnosis of upper gastrointestinal disease combined with endoscopic findings and pathological diagnosis. Within two weeks after receiving the survey
Secondary The infection rate of Helicobacter Pylori H. pylori infection was determined by any two of positive outcome of the breath test, rapid urease test and histology. Within two weeks after receiving the survey
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