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Safety and Efficacy of Snare-assisted Endoscopic Submucosal Tunneling Dissection for Esophageal Submucosal Tumors: A Prospective, Multi-center, Randomized Controlled Trial

Safety and Efficacy of Snare-assisted Endoscopic Submucosal Tunneling Dissection for Esophageal Submucosal Tumors: A Prospective, Multi-center, Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064442
Enrollment
Unknown
Registered
2022-10-08
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Esophageal submucosal tumor

Interventions

Traction group:Tunnel ESD with Snare based tration
Control group:Tunnel ESD

Sponsors

Department of Gastroenterology, the First Hospital of Nanchang (The Third Affiliated Hospital of Nanchang University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years; 2. Submucosal lesions were found in the esophagus, which were confirmed by endoscopic ultrasound to be from the musculi propria; 3. The transverse diameter of the tumor evaluated by CT or endoscopic ultrasound was 1cm-3cm; 4. No history of esophageal operation and previous treatment; 5. Able to understand and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Other malignant tumors are diagnosed, and the survival time is less than 6 months according to the attending doctor; 2. Patients unable to undergo endoscopic treatment due to anatomical structure changes caused by digestive tract operations or combined digestive tract diseases; 3. ASA>=4; 4. Patients with abnormal coagulation function, such as thrombocytopenia or abnormal coagulation caused by blood system diseases or taking aspirin and other anticoagulant drugs; 5. Patients with severe heart, liver and kidney insufficiency; 6. Patients who are pregnant, planning to become pregnant, or breastfeeding.

Design outcomes

Secondary

MeasureTime frame
En bloc resection;Hospital stay;Complete healing rate;

Primary

MeasureTime frame
Procedural time;

Countries

China

Contacts

Public ContactFang Nian

Department of Gastroenterology, the First Hospital of Nanchang (The Third Affiliated Hospital of Nanchang University)

fangnian_ncu@163.com+86 13892812764

Outcome results

None listed

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