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A study on the effectiveness and safety of a new device of closure for large defect after endoscopic therapy

A study on the effectiveness and safety of a new device of closure for large defect after endoscopic therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081229
Enrollment
Unknown
Registered
2024-02-27
Start date
2024-02-27
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Lesion of digestive tract

Interventions

Sponsors

Shengjing hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Patients =18 years old 2) Endoscopic mucosal resection, Endoscopic submucosal dissection or Endoscopic full-thickness resection were performed., the defect size was =2cm and need to be closed 3) Have a full understanding of the study and signed the informed consent

Exclusion criteria

Exclusion criteria: 1) There is contraindication of endoscopic procedure; 2) Coagulation dysfunction (INR=1.5, platelet < 50 × 109/L); 3) Preoperative endoscopic ultrasonography or abdominal CT evaluation showed obvious malignant signs (tumor accompanied by ulcers, cystic changes, lymph node enlargement, invasion of adjacent organs and tissues, etc.) to rule out extrinsic pressure lesions, such as gallbladder and mutated blood vessels; 4) Refuse to sign the informed consent.

Design outcomes

Primary

MeasureTime frame
Success rate of complete closure;

Secondary

MeasureTime frame
Adverse events;

Countries

China

Contacts

Public ContactGe Nan

Shengjing Hospital affiliated to China Medical University

2924922897@qq.com+86 133 2247 5770

Outcome results

None listed

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