Quality of Life in Barrett's Esophagus and Gastro-Esophageal Reflux Disease
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT01572974 |
Recruitment Status
:
Terminated
(Lack of recruitment)
First Posted
: April 6, 2012
Last Update Posted
: January 18, 2018
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease |
---|
Barrett's Esophagus Gastroesophageal Reflux Disease |
Study Type : | Observational |
Actual Enrollment : | 89 participants |
Observational Model: | Case-Only |
Time Perspective: | Prospective |
Official Title: | Quality of Life in Barrett's Esophagus and GERD:GERD Symptoms, Perception of Cancer Risk, and Actual Cancer Risk |
Study Start Date : | January 2010 |
Actual Primary Completion Date : | September 2016 |
Actual Study Completion Date : | December 2017 |

Group/Cohort |
---|
No Barrett's esophagus
Subject without columnar lined esophagus
|
Nondysplastic BE
Subject with columnar lined esophagus and absence of dysplasia
|
Low grade dysplastic BE
subject with columnar lined esophagus and presence of low grade dysplasia
|
High grade dysplastic BE
subject with columnar lined esophagus and presence of high grade dysplasia
|
- Health State Utility as measured by the Time Trade-off (TTO) method/Standard Gamble (SG) method [ Time Frame: 1 year ]questionnaire
- SF-36 physical function (PF) subscale [ Time Frame: 12 months ]questionnaire
- SF-36 role limitations-physical (RP) subscale [ Time Frame: 12 months ]questionnaire
- SF-36 general health (GH) subscale [ Time Frame: 12 months ]questionnaire

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years and older (Adult, Senior) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
Inclusion Criteria:
Age 18 or above
At least one of the following:
Previous diagnosis of Barrett's esophagus Presence of GERD symptoms per patient report
Exclusion Criteria:

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01572974
United States, Missouri | |
Kansas City VA Medical Center | |
Kansas City, Missouri, United States, 64128 |
Principal Investigator: | Prateek Sharma, MD | Kansas City VA Medical Center |
Publications:
Responsible Party: | PRATEEK SHARMA, Principal Investigator, Midwest Biomedical Research Foundation |
ClinicalTrials.gov Identifier: | NCT01572974 History of Changes |
Other Study ID Numbers: |
PS0056 |
First Posted: | April 6, 2012 Key Record Dates |
Last Update Posted: | January 18, 2018 |
Last Verified: | January 2018 |
Keywords provided by PRATEEK SHARMA, Midwest Biomedical Research Foundation:
Barrett's esophagus Gastroesophageal reflux disease Quality of life |
Additional relevant MeSH terms:
Gastroesophageal Reflux Barrett Esophagus Esophageal Motility Disorders Deglutition Disorders |
Esophageal Diseases Gastrointestinal Diseases Digestive System Diseases Digestive System Abnormalities |