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Clinical Trials of Disposable Gastroscope for Upper Gastrointestinal Emergency Bedside and Intraoperative Diagnosis and Treatment

Clinical Trials of Disposable Gastroscope for Upper Gastrointestinal Emergency Bedside and Intraoperative Diagnosis and Treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051452
Enrollment
Unknown
Registered
2021-09-23
Start date
2021-09-30
Completion date
Unknown
Last updated
2022-06-20

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

Conditions

Upper Gastrointestinal Disease

Interventions

Experimental group:XZING-W200B

Sponsors

Nanfang Hospital, Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years, without gender limitation; 2. Gastroscopic diagnosis and/or treatment are needed during gastrointestinal emergency and surgery; 3. Participate in the clinical trial voluntarily with the signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications to upper gastrointestinal endoscopy: (1) Those with thoracic and abdominal aortic aneurysms; (2) Those with a high degree of spinal deformity; (3) Patients with severe cardiovascular and cerebrovascular diseases; (4) Severe cardiopulmonary insufficiency is expected to be unable to tolerate gastroscopy; (5) Combined with systemic hemorrhagic diseases, or those with abnormal coagulation function and bleeding tendency; (6) Those with mental illness or severe intellectual disability who cannot cooperate with endoscopy. 2. Pregnant and lactating women; 3. Those who participated in other clinical trials one month before screening; 4. Those who have a history of allergy to anesthetics in the past; 5. Patients who are judged by the investigator to be unsuitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Timely detection of lesions and evaluation on handling capability;

Secondary

MeasureTime frame
Evaluation on clinical operational experience ;

Countries

China

Contacts

Public ContactLiu Side

Nanfang Hospital, Southern Medical University

liuside@163.com+86 13902212459

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026