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Optimal surveillance interval after endoscopic submucosal dissection-a multicenter prospective cohort study comparing biannual and annual follow up

Optimal surveillance interval after endoscopic submucosal dissection-a multicenter prospective cohort study comparing biannual and annual follow up

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0003409
Enrollment
540
Registered
2018-12-27
Start date
2018-03-26
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Procedure/Surgery : Of patients who have undergone endoscopic resection for gastric neoplasms, patients with curative resection were enrolled. The 6-month follow-up group (biannual group) will be fol

Sponsors

The Catholic University of Korea, Incheon St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who underwent endoscopic resection for gastric neoplasms(early gastric cancer or dysplasia) 2. Patients who meet criteria for curative resection 3. Patients 20 to 80 years old who agreed to the study

Exclusion criteria

Exclusion criteria: 1. Patients with a past history of gastric surgery 2. Patients with a history of endoscopic resection 3. Patients with severe cirrhosis 4. Patients with bleeding tendency 5. Pregnant women 6. patients who can't obtain consent

Design outcomes

Primary

MeasureTime frame
incidence of metachronous lesion

Secondary

MeasureTime frame
curative resection of metachronous lesion

Countries

Korea, Republic of

Contacts

Public ContactCheal Wung Huh

The Catholic University of Korea, Incheon St. Mary's Hospital

gjcjfdnd01@naver.com+82-32-280-5052

Outcome results

None listed

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