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Evaluation of Efficacy and Safety of Medical Disposable Portable Endoscopic System in Human Experiment

Evaluation of Efficacy and Safety of Medical Disposable Portable Endoscopic System in Human Experiment

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000038516
Enrollment
Unknown
Registered
2020-09-23
Start date
2020-09-18
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

gastrointestinal disease

Interventions

Gold Standard:Olympus endoscopic diagnosis and treatment

Sponsors

The First Medical Center, Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Physical condition of participants meets the requirements of endoscopy; 2. Participants of 18-75 years old; 3. Participants who are informed and consent and volunteer to participate; 4. Participants who sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Participants with past history: Medical history of upper gastrointestinal surgery; 2. Participants with history of present illness: active ulcers, atypical hyperplasia, dysphagia, iron-deficiency anemia, damage to vital organs, unstable cardiopulmonary diseases, endocrine diseases, malignant tumors, and patients with incorrect expression of chief complaints, such as mental diseases and neurosis; 3. Participants who take corticosteroids, NSAID, anticoagulants and antiplatelet aggregation drugs; 4. Female participants who are pregnant or lactating; 5. Participants unable to cooperate with follow-up.

Design outcomes

Primary

MeasureTime frame
the operation time;Image quality;operation performance;Detected Lesions and Safety Evaluation;endoscopic therapeutic effect;

Countries

China

Contacts

Public ContactYunsheng Yang

The First Medical Center, Chinese PLA General Hospital

sunnyddc@plagh.org+86 13910767280

Outcome results

None listed

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