Efficacy of re-examination of stomach for detection of metachronous lesions: a randomized controlled trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002797

Enrollment

630

Registered

2018-04-14

Start date

2017-06-05

Completion date

Unknown

Last updated

2023-01-10

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 : ? In patients with endoscopic resection, - Patients undergoing endoscopic resection will undergo a follow-up endoscopy within 8-12 weeks after the procedure and will be tested at i

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Patients who fully understand the purpose of this study and agree to participate in this study - Patients who underwent endoscopic resection for endometrial lesions such as adenoma and early gastric cancer and underwent follow-up endoscopy

Exclusion criteria

Exclusion criteria: - Patients who underwent stomach surgery - If the patient does not agree to participate in the study -American Society of Anesthesiologists (ASA) score of 5 or higher

Design outcomes

Primary

Measure	Time frame
Percentage of synchronous lesions and metachronous lesions	—

Secondary

Measure	Time frame
Endoscopy time;Number and diagnosis of biopsy	—

Countries

Korea, Republic of

Contacts

Public ContactJoon Sung Kim

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

kijoons@hanmail.net+82-32-280-5054

Outcome results