Incidence & Clinical Course of Colonoscopy Related Perforation

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Perforation Colon

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

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

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03833856
Study type	Observational [Patient Registry]
Source	Kyungpook National University Hospital
Contact
Status	Completed
Phase
Start date	January 1, 2017
Completion date	January 2021

Incidence and Clinical Course of Colonoscopy Related Perforation

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms