Skip to content

Comparison of the efficacy of modified interrupted closure technique and traditional closure technique in endoscopic full-thickness resection

Comparison of the efficacy of modified interrupted closure technique and traditional closure technique in endoscopic full-thickness resection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086500
Enrollment
Unknown
Registered
2024-07-03
Start date
2023-09-27
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

submucosal tumors

Interventions

experimental group:interrupted suture
Control group·:traditional closure

Sponsors

General Hospital of Northern Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-80 years old. 2. Endoscopic ultrasonography confirmed gastric submucosal tumor. 3. No definite metastasis was found by imaging examination. 4. The maximum cross-sectional diameter of the lesion is =5.0cm. 5. Voluntarily participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Submucosal tumor surface rupture. 2. Multiple EFTR treatments were performed. 3. Allergic to lidocaine mucilage, strepase protease and simethicone. 4. You are pregnant or breastfeeding. 5. Known clotting disorders (including thrombocytopenia, hemophilia, von willebrand disease, etc.) or use of anticoagulants or antiplatelet drugs can not be stopped. 6. Other systemic malignancies. 7. Mental and neurological diseases, serious heart and lung diseases, liver and kidney diseases, immune and blood system diseases, electrolyte disorders. 8. Preoperative American Society of Anesthesiologists (ASA) grade =IV. 9. Participants who participated in other clinical trials 3 months before surgery or during the trial. 10. The researcher considers it inappropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative minor complications;

Secondary

MeasureTime frame
Complete resection rate;Duration of surgery;Incidence of intraoperative bleeding;

Countries

China

Contacts

Public Contactzhuo yang

General Hospital of Northern Theater Command

yangzhuocy@163.com+86 133 0988 8172

Outcome results

None listed

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