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Transanal Tube Drainage in the Prevention of Electrocoagulation Syndrome after Endoscopic Submucosal Dissection for Colorectal Lesions: A Prospective, Multi-Center, Randomized, Open-Label, Parallel Group, Superiority Clinical Trial

Transanal Tube Drainage in the Prevention of Electrocoagulation Syndrome after Endoscopic Submucosal Dissection for Colorectal Lesions: A Prospective, Multi-Center, Randomized, Open-Label, Parallel Group, Superiority Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062164
Enrollment
Unknown
Registered
2022-07-26
Start date
2022-07-12
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Colorectal mucosal lesions

Interventions

test group:Transanal Tube Drainage

Sponsors

Zhongshan Hospital affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age > 18 years old; 2.Preoperative colonoscopy or ultrasonic endoscopic assessment suitable for patients with ESD; 3.Endoscopic examination of mucous membrane lesions with large =2cm; 4.No combined with colorectal disease; 5.Single ESD resection a single lesion; 6.Patients or family members can understand the research plan and are willing to participate in this study and provide written knowledge consent.

Exclusion criteria

Exclusion criteria: 1.Age <18 years old; 2.Patients with intestinal diseases of colorectal and intestinal diseases at the same time; 3.Patients with family interest meat disease; 4.The history of colorectal surgery in the past may affect the patients post-operation outcome 5.Women of pregnancy or lactation: 6.Those with severe emphysema, interstitial pneumonia or ischemic heart disease cannot withstand anesthesia and surgical; 7.Patients transfer to surgery; 8.Patients have taboos of ESD; 9.Patients or family members cannot understand the conditions and goals of this study

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative electrocoagulation syndrome;

Secondary

MeasureTime frame
Incidence of postoperative bleeding perforation;VAS score;Postoperative laboratory examination;Postoperative hospital stay;Postoperative maximum body temperature;

Countries

China

Contacts

Public ContactZhong Yunshi
20211210043@fudan.edu.cn13564623481

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026