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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03833856
Other study ID # KNUH2019
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2017
Est. completion date January 2021

Study information

Verified date January 2021
Source Kyungpook National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This study aims to investigate the incidence and clinical course of colonoscopy related perforation based on the result of a prospective registry.


Description:

In each endoscopy unit from participating hospital, there is a alarm system focusing on the development of perforation. Therefore, perforation cases will not be missed from the registry.


Recruitment information / eligibility

Status Completed
Enrollment 58
Est. completion date January 2021
Est. primary completion date August 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients who have a perforation after colonoscopy Exclusion Criteria: - Patients who refuse to be registered.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
colonoscopy perforation
The development of perforation after colonoscopy

Locations

Country Name City State
Korea, Republic of Kyungpook National University Hospital Daegu

Sponsors (1)

Lead Sponsor Collaborator
Kyungpook National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Operation Number of participants who take surgical treatment after perforation 1 month
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05728710 - Outcomes of Perforation After Colorectal Endoscopic Submucosal Dissection
Recruiting NCT05653843 - MANTIS Endoscopic Clipping Study
Recruiting NCT05852457 - Evaluation of the Clinical Utility of Endoscopic Closure Using a Dual Action Tissue (DAT) Clip