Skip to content

Evaluation of a portable disposable gastroenteroscopy system in the examination and treatment of acute gastrointestinal bleeding

Evaluation of a portable disposable gastroenteroscopy system in the examination and treatment of acute gastrointestinal bleeding

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090157
Enrollment
Unknown
Registered
2024-09-25
Start date
2023-04-07
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

Acute gastrointestinal bleeding

Interventions

portable disposable gastroenteroscopy group:portable disposable gastroenteroscopy
Reusable endoscope group:Reusable endoscope

Sponsors

PLA Strategic Support Force Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
29 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: (1) Age 18-90 years old, gender is not limited; (2) Gastrointestinal bleeding (estimated to be around 800ml) requires emergency bedside gastroscopy or colonoscopy and/or treatment; (3) Voluntarily participate in this clinical trial and have signed a written informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion criteria: (1) Patients with contraindications to the diagnosis and treatment of gastrointestinal endoscopy; Patients with thoracoabdominal aortic aneurysm;?Those with high spinal deformity;?Patients with severe cardiovascular and cerebrovascular diseases;?Patients with severe cardiopulmonary insufficiency who are expected to be unable to tolerate gastroscopy; ?Patients with systemic bleeding disorders, or abnormal coagulation function and bleeding tendency;?Those who have mental illness or severe intellectual disability and cannot cooperate with endoscopy; (2)Pregnant and lactating females;(3)Those who have participated in other clinical trials 1 month before screening;(4) Those who have a history of allergy to anesthetic drugs in the past;(5) Patients who are judged by the investigator to be unsuitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Technical success rate;

Secondary

MeasureTime frame
Image quality score;Clinical operation evaluation;Equipment preparation time and transportation time;Device failure/defect rate ;Incidence of adverse events;

Countries

China

Contacts

Public ContactLianyong Li

Department of Gastroenterology, PLA Strategic Support Force Medical Center

lilianyong001@163.com+86 138 1058 4399

Outcome results

None listed

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