Long Term Barrett's Endoscopic Mucosal Resection Study

See also
Status	Clinical Trial	Phase
Completed	`NCT00650988` - Cryotherapy for Barrett's Esophagus and Early Esophageal Cancers	Phase 0
Completed	`NCT01733719` - Barrett&Apos;s Intervention for Dysplasia by Endoscopy	N/A
Completed	`NCT00586989` - Endoscopic Tri-Modal Imaging in Patients With Barrett's Esophagus	N/A
Terminated	`NCT00737802` - In Vivo Anatomy, Physiology, Mechanics and Function of the Lower Esophageal Sphincter

See also

Status

Clinical Trial

Phase

Completed

NCT00650988 - Cryotherapy for Barrett's Esophagus and Early Esophageal Cancers

Phase 0

Completed

NCT01733719 - Barrett&Apos;s Intervention for Dysplasia by Endoscopy

N/A

Completed

NCT00586989 - Endoscopic Tri-Modal Imaging in Patients With Barrett's Esophagus

N/A

Terminated

NCT00737802 - In Vivo Anatomy, Physiology, Mechanics and Function of the Lower Esophageal Sphincter

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	NCT02200250
Study type	Observational
Source	Western Sydney Local Health District
Contact
Status	Withdrawn
Phase
Start date	October 1, 2021
Completion date	October 2022

Long Term Barrett's Endoscopic Mucosal Resection Study — CBE

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms