Risk of high-grade dysplasia or carcinoma in gastric biopsy-proven low-grade dysplasia: an analysis using the Vienna classification.
S-J Cho, I J Choi, C G Kim...
https://pubmed.ncbi.nlm.nih.gov/21425043/Actively Recruiting
Led by Samsung Medical Center · Updated on 2026-02-06
160
Participants Needed
3
Research Sites
8 weeks
Total Duration
Gastric adenomas with low-grade dysplasia LGD are precancerous stomach lesions with a lower risk of progressing to cancer compared to high-grade dysplasia. This trial aims to compare two common endoscopic treatments, argon plasma coagulation APC and endoscopic mucosal resection EMR, to see if APC is as effective as EMR in preventing local recurrence of these small lesions measuring 1 cm or less. The study addresses current uncertainties and differing international guidelines on managing these lesions. Participants will be randomly assigned to receive either APC, which uses ionized argon gas to coagulate tissue without cutting, or EMR, which involves lifting and cutting out the lesion. EMR allows detailed pathological examination but may take longer and have more complications, while APC is simpler, quicker, and usually less invasive but lacks tissue for pathology. After treatment, all participants receive standard medical care and are monitored for any complications. Participants will return for follow-up endoscopies at 3 and 12 months to check the treated area and take biopsies if needed to detect recurrence. Researchers will record the local recurrence rate at 12 months as the main outcome, along with procedure-related complications like bleeding or perforation, procedure time, and recovery experience. The trial will provide important evidence to guide treatment choices for patients with small gastric adenomas.
CONDITIONS
Argon Plasma Coagulation Versus Endoscopic Mucosal Resection for Gastric Adenoma (CLER-GA)
C
Clinical Research Coordinator
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Samsung Medical Center
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of procedure
Participants undergo either argon plasma coagulation or endoscopic mucosal resection to treat gastric adenoma measuring 1 cm or smaller.
1 treatment visit (in-person)
Duration - 12 months
Participants are monitored with surveillance endoscopies to assess the treated site and check for recurrence.
2 visits (at 3 months and 12 months, in-person)
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Have more questions? Get in touch with our team for quick support
S-J Cho, I J Choi, C G Kim...
https://pubmed.ncbi.nlm.nih.gov/21425043/Pedro Pimentel-Nunes, Diogo Libânio, Barbara A J Bastiaansen...
https://pubmed.ncbi.nlm.nih.gov/35523224/Guangfeng Zhao, Meng Xue, Yingying Hu...
https://pubmed.ncbi.nlm.nih.gov/26182344/Se Jin Jung, Soo-Jeong Cho, Il Ju Choi...
https://pubmed.ncbi.nlm.nih.gov/23076459/In-Ho Kim, Seung Joo Kang, Wonyoung Choi...
https://pubmed.ncbi.nlm.nih.gov/39822170/Samsung Medical Center
Lead Sponsor