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Efficacy and Safety Study of Endoscopic Submucosal Dissection for Early Gastric Cancer

Long-term Follow-up After Endoscopic Submucosal Dissection for Early Gastric Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01132469
Acronym
ESD
Enrollment
1158
Registered
2010-05-28
Start date
2010-05-31
Completion date
2017-06-30
Last updated
2010-05-28

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

Conditions

Early Gastric Cancer, Endoscopic Submucosal Dissection, Historical Control Group, Multi-center, Single-arm Clinical Trial, Quality of Life and Cost Analysis

Brief summary

The purpose of this study is to evaluate the safety and clinical effectiveness of ESD(Endoscopic Submucosal Dissection) for early gastric cancer analyzing short-term and long-term results of endoscopic treatment.

Detailed description

Traditionally open-gastrectomy is the standard treatment for gastric cancer without distant metastasis, but high mortality and morbidity, the intense weight loss, food intake difficulties after surgery are fraught, including problems with the drawback of significantly degrading the quality of life. Therefore, a lot of effort to seek the more simple treatment than open gastrectomy has been made, recently the endoscopic treatment for early gastric cancer is the most widely used treatment. This single-arm, multi-center study enroll early gastric cancer patients after ESD compared with the retrospective control(surgical treatment) group considering the unreality of the randomized clinical trials. In addition, the quality of life assessment by the EORTC C30/STO22 tools before and after ESD procedure in enrolled patients will be performed and the direct cost analysis also will be conducted.

Interventions

PROCEDUREEndoscopic Submucosal Dissection

5-years follow-up after Endoscopic Submucosal Dissection

Sponsors

National Evidence-Based Healthcare Collaborating Agency
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. ESD GROUP Inclusion Criteria: * Korean people aged \>=20 years * Endoscopic Grossly the lesion diameter ≤ 3cm * Endoscopic biopsy results: Well-differentiated and moderately differentiated adenocarcinoma * No ulcers in lesions * Endoscopic biopsy results: In case of gastric cancer, no metastasis in CT test performed before ESD procedure

Exclusion criteria

* Subject with history of malignant disease in other organs * Subject with history of stomach surgery due to peptic ulceration etc. * As the cases of an absolute contraindication of general anesthesia; Subject with chronic liver disease over Child score B, Subject with chronic Renal Disease requiring hemodialysis or peritoneal dialysis, Subject with heart failure more than Ⅲ score according to New York Heart Association Classification, Subject with severe systemic diseases such as respiratory disease * Subject with Bleeding tendency * Pregnant woman or woman with possibility of pregnancy * Subject who cann't be obtained informed consent * Subject who is unable to follow up for any other reason 2. Surgery Group(Retrospective data collection) Inclusion Criteria: * Subject with gastric laparoscopy or open-surgery for treatment early gastric cancer during 2002.1.1 \ 2004. 12. 31 * Korean people aged \>=20 years * Early gastric cancer confirmed by pathology during gastric surgery; Gastric cancer confirmed to the mucosal or submucosal regardless of lymph node metastasis * No history of malignant disease in other organs * No history of stomach surgery due to peptic ulceration etc.

Design outcomes

Primary

MeasureTime frame
5-year disease(gastric cancer)-free survival rate after ESD procedure5 years after ESD

Secondary

MeasureTime frame
Short-term result(Histological complete resection,complication)within the first 7 days after ESD
The incidence of reoccurrence and Ectopic fociwithin the first 7 days and 3months, 6months, 1year, 2years, 3years, 4years and 5years after ESD
The quality of life after ESDbefore and 7 days, 3months, 6months after ESD
The costs of ESDFrom the admission to discharge
The safety of ESD procedurewithin the 7 days, 3months, 6months, 1year, 2years, 3years, 4years and 5years after ESD

Countries

South Korea

Contacts

Primary ContactEunhee Shin, Ph.D.
hshin@neca.re.kr82-2-2174-2740
Backup ContactJonghee Kim, MS
goldpaper2@neca.re.kr82-2-2174-2742

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026