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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03833492
Other study ID # UEMR-1.0
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2019
Est. completion date November 12, 2019

Study information

Verified date December 2019
Source Ningbo No. 1 Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This clinical trial is being conducted to compare the efficacy and safety of two standard methods of polypectomy,Conventional Endoscopic Mucosal Resection(EMR)and Underwater Endoscopic Mucosal Resection(UEMR),for small colorectal polyps.


Recruitment information / eligibility

Status Completed
Enrollment 130
Est. completion date November 12, 2019
Est. primary completion date November 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

Patients age between 18-75 years old with non-pedunculated colonic polyps (measuring between 4 and 9mm), who willing to participate in this study.

Exclusion Criteria:

1. pregnancy,

2. inflammatory bowel disease,

3. familial polyposis

4. the use of anticoagulant therapy or antiplatelet therapy

5. the absence of informed patient consent.

6. Polyps showing signs of deep submucosal invasion

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Underwater EMR
Polypectomy is performed under full water emersion without the use of submucosal injection.

Locations

Country Name City State
China Department of Gastroenterology, Haishu No.2 Hospital, Ningbo, China Ningbo Zhejiang
China Department of Gastroenterology, Ninghai No.2 Hospital, Ningbo, China Ningbo Zhejiang
China Ningbo first hospital Ningbo Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Ningbo No. 1 Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary complete resection rate complete resection rate is defined as a complete en bloc resection of a lesion with tumor-free lateral and vertical margins. 7 days
Primary En bloc resection rate En bloc resection rate was defined as the entire lesion could be removed in 1 piece instead of piecemeal resection. immediately
Secondary Adverse event rate Including bleeding and perforation , etc. 14 days
Secondary Procedure time Time to execute the program 24 hours
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