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A prospective study on novel suturing device for closure of large post-endoscopic resection wounds

A prospective study on novel suturing device for closure of large post-endoscopic resection wounds

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107400
Enrollment
Unknown
Registered
2025-08-11
Start date
2025-08-15
Completion date
Unknown
Last updated
2025-08-18

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

new device group:Closure of wounds using a novel suturing device

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) wounds exceeding 3 cm resulting from non-full-thickness resection or wounds (including fistulae) exceeding 1 cm resulting from full-thickness resection required suturing; (2) age between 18 and 80 years; (3) provision of written informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: (1) Presence of contraindications to endoscopic procedures; (2) Inability to discontinue anticoagulants or antiplatelet agents; (3) Preoperative examinations indicating definite distant metastasis or lymph node metastasis; (4) Refusal to participate in the study and signing of a written informed consent form; (5) Other circumstances deemed ineligible for enrollment by the endoscopist.

Design outcomes

Primary

MeasureTime frame
Success rate of complete closure;

Secondary

MeasureTime frame
Closure time;Adverse events;

Countries

China

Contacts

Public ContactZhai Yaqi

Chinese PLA General Hospital

astaring@163.com+86 138 1010 5934

Outcome results

None listed

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