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A Study on the Application of Lateral Multi-lumen Drainage Tubes in the Prevention of PECS of Mucosal Lesions in the Right Half of the Colon: A Prospective, Multicentre, Stratified, Randomised, Open-label, Parallel-group Superiority Trial

A Study on the Application of Lateral Multi-lumen Drainage Tubes in the Prevention of PECS of Mucosal Lesions in the Right Half of the Colon: A Prospective, Multicentre, Stratified, Randomised, Open-label, Parallel-group Superiority Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123849
Enrollment
Unknown
Registered
2026-04-30
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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:Lateral Multi-lumen Tube Drainage

Sponsors

Shanghai Xuhui Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age > 18 years; 2. American Society of Anesthesiologists (ASA) Class I–III; 3. Patients deemed suitable for ESD following preoperative colonoscopy or endoscopic ultrasound assessment; 4. Endoscopically identified mucosal lesions >= 2 cm in size located in the right half of the colon; 5. No concomitant organic diseases of the colon or rectum; 6. Resection of a single lesion via a single ESD procedure; 7. The patient or their family members are able to understand the study protocol, are willing to participate in this study, and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Age < 18 years; 2. Patients with concomitant organic diseases of the colon or rectum; 3. Patients with familial polyposis; 4. Patients with a history of colorectal surgery that may affect the outcome of the current procedure; 5. Pregnant or breastfeeding women; 6. Patients with severe emphysema, interstitial pneumonia or ischaemic heart disease who cannot tolerate anaesthesia or surgery; 7. Patients requiring conversion to open surgery; 8. Patients with contraindications to ESD surgery; 9. Patients or their relatives who are unable to understand the conditions and objectives 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

Zhongshan Hospital affiliated to Fudan University

zhong.yunshi@zs-hospital.sh.cn+86 135 6462 3481

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026