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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04197180
Other study ID # CREC 2019.490-T
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 1, 2020
Est. completion date December 31, 2024

Study information

Verified date November 2023
Source Chinese University of Hong Kong
Contact Philip WU Chiu, MD
Phone +85235053952
Email philipchiu@surgery.cuhk.edu.hk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This cohort study aims to investigate the clinical efficacy and safety of Hybrid APC for treatment of gastric low grade intramucosal neoplasia.


Description:

This cohort study aims to investigate the clinical efficacy and safety of Hybrid APC for treatment of gastric low grade intramucosal neoplasia. Successful ablation is defined as no evidence of local recurrence at 12 months after HybridAPC upon follow up endoscopy. This is defined as absence of LGIN, HGIN and cancer in biopsies obtained at all locations during followup endoscopy.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: 1. Low grade intraepithelial neoplasia of stomach with size=20 mm 2. Endoscopic diagnosis suspected gastric LGIN with biopsy confirmed gastric LGIN 3. Endoscopic appearance according to Paris classification of Type 0-IIa, IIb or IIc 4. Patients with informed consent Exclusion Criteria: 1. Patients who had previous endoscopic treatment (including APC, EMR, ESD) for gastric LGIN, HGIN or gastric carcinoma. 2. Endoscopic evidence of ulcer 3. Biopsy confirmed HGIN 4. Endoscopic diagnosis suspected HGIN while biopsy confirmed LGIN 5. Pregnancy 6. informed consent not available

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Hybrid Argon Plasma Coagulation
Argon Plasma Coagulation after water injection for local ablation

Locations

Country Name City State
Hong Kong Combined Endoscopy Center, Prince of Wales Hospital Hong Kong

Sponsors (4)

Lead Sponsor Collaborator
Chinese University of Hong Kong Nanfang Hospital, Southern Medical University, Shenzhen Hospital of Southern Medical University, The Fifth Affiliated Hospital of Zunyi Medical College

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary Complete ablation of gastric low grade intraepithelial neoplasia Successful ablation is defined as no evidence of local recurrence at 12 months after HybridAPC upon follow up endoscopy. This is defined as absence of LGIN, HGIN and cancer in biopsies obtained at all locations during followup endoscopy. 12 months
Secondary Operative time Time to complete the procedure 1 day
Secondary Intraoperative bleeding Bleeding during the procedure as defined by Grade Definition 0 No bleeding
Less bleeding, could be auto-stopped or used by HibridAPC
Stop bleeding by using hot forceps
Stop bleeding by using clips
1 day
Secondary Pain after procedure Pain after the procedure as defined by pain score Grade Definition 0 No pain, I Slight pain, II Moderate pain, III Severe pain, IV Extreme pain. V Unbearable pain 3 days
Secondary Development of new neoplasia Development of new neoplasia including low grade intraepithelial neoplasia, high grade intraepithelial neoplasia and advanced gastric cancers 12, 24 and 36 months
Secondary Progression of Low grade intraepithelial neoplasia Progression of the development of low grade intraepithelial neoplasia to high grade intraepithelial neoplasia or advanced gastric cancer 12, 24 and 36 months
Secondary Postoperative complications Development of postoperative complications including bleeding and perforation 7 days
Secondary Number of HybridAPC procedures required for treatment The number of Hybrid Argon Plasma Coagulation performed for complete ablation 12 months