Skip to content

Clinical Trial of Disposable Gastroscope for Upper Gastrointestinal Examination and Treatment with EndoTherapy Accessories

Clinical Trial of Disposable Gastroscope for Upper Gastrointestinal Examination and Treatment with EndoTherapy Accessories

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040634
Enrollment
Unknown
Registered
2020-12-04
Start date
2021-01-04
Completion date
Unknown
Last updated
2021-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Upper Gastrointestinal Disease

Interventions

Group 1:XZING-W200B Gastroscopy+Biopsy+EMR
Group 2:GIF-HQ290+Biopsy+EMR

Sponsors

HuiZhou Xzing Technology Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The age ranged from 18 to 75 years old; 2. Painless gastroscopy and / or treatment are needed; 3. Participate in the clinical trial voluntarily, and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications for gastroscopy: (1) patients with thoracic and abdominal aortic aneurysm; (2) patients with high spinal deformity; (3) severe cardiovascular and cerebrovascular diseases; (4) Patients with functional insufficiency who can not tolerate gastroscopy; (5) patients with huge diverticulum of upper digestive tract; (6) patients with acute upper gastrointestinal inflammation; (7) patients with systemic hemorrhagic diseases; (8) patients with mental illness or severe mental retardation who cannot cooperate with endoscopy; 2. Pregnant and lactating women; 3. Emergency gastroscopy and / or treatment; 4. Patients with previous history of upper gastrointestinal surgery; 5. Those who participated in other clinical trials one month before screening; 6. Patients who need other gastrointestinal endoscopy and / or treatment on the same day; 7. Patients with previous history of allergy to narcotic drugs; 8. The researcher thinks that it is not suitable to participate in this experiment.

Design outcomes

Primary

MeasureTime frame
Qulification rate of image evaluation;AE Incidence Rate;Operating Time;

Secondary

MeasureTime frame
Image Quality Scoring;Failure rate;

Countries

China

Contacts

Public ContactPeng Li

Capital Medical University Affiliated Beijing Friendship Hospital

lipeng@ccmu.edu.cn+86 010-63139206

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026