Prospective observational study on the time of electrocoagulation use during colorectal endoscopic submucosal dissection

Prospective observational study on the time of electrocoagulation use during colorectal endoscopic submucosal dissection - Prospective observational study on the time of electrocoagulation use during colorectal endoscopic submucosal dissection

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000041580

Enrollment

Registered

2020-08-27

Start date

2020-08-26

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Colorectal tumor

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Colorectal tumor patients who are eligible for colorectal ESD Those who are 20 years of age or older at the time of hospitalization

Exclusion criteria

Exclusion criteria: Patients with metastases Those who are complicated by intestinal ischemia and necrosis

Design outcomes

Primary

Measure	Time frame
Onset of post-ESD electrocoagulation syndrome	—

Countries

Japan

Contacts

Public ContactMasanori Ochi

Hitachi General Hospital Department of Gastroenterology

maochi-tei@umin.ac.jp0294231111

Outcome results