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Study of Capsule Endoscopy to Determine the Accuracy for Detection of Esophageal Varices

Is Capsule Endoscopy Accurate and Cost-effective Enough to Screen Cirrhotic Patients for Varices & Other Lesions?

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01079416
Enrollment
65
Registered
2010-03-03
Start date
2006-06-30
Completion date
2008-02-29
Last updated
2013-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Varices

Keywords

Esophageal Capsule Endoscopy, Screening

Brief summary

Esophageal capsule endoscopy is sedation-less alternative to upper endoscopy for evaluating esophageal lesions and potentially other upper gastrointestinal lesions. The purpose of this study was to determine whether esophageal capsule endoscopy is convenient and accurate as upper endoscopy for detection of esophageal varices and related lesions.

Interventions

DEVICECapsule endoscopy, Esophagogastroduodenoscopy

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
University of California, Los Angeles
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Age at least 18 years and less than 86 years at the time of consent. * Clinically evident or biopsy proven cirrhosis. * No previous documented UGI bleeding due to peptic ulcers, varices, portal hypertensive gastropathy, angiomas, or watermelon stomach. * No previous endoscopic, radiological or surgical treatment for variceal bleeding or ascites. * Probable life expectancy of at least 24 months without liver transplantation, as judged by the hepatologist and endoscopist-investigators, and have a Model for End-Stage Liver Disease (MELD) score ≤ 29. * Signed a written informed consent.

Exclusion criteria

* Prior variceal bleeding- esophageal, gastric, or other site. * Prior endoscopic (e.g. sclerotherapy, ligation, or combination therapy), radiological (e.g. transjugular intrahepatic portosystemic shunt-TIPS) or surgical (e.g. portocaval or splenorenal shunt) treatment of esophagogastric varices or ascites. * Patient who was uncooperative or unable to give written consent. * Severe co-morbid illness, e.g. end stage chronic renal disease (e.g. dialysis dependence, creatinine greater than 2 times normal) or respiratory failure (e.g. ventilator dependent, oxygen dependent, unstable asthma or chronic obstructive pulmonary disease- e.g. 2 or more hospitalizations for exacerbation in 1 year, asthma or obstructive pulmonary disease which required daily bronchodilators and/or oral/inhaled steroids), tense ascites requiring repeated therapeutic paracenteses, severe hepatic encephalopathy, peritonitis, or sepsis. * Active cancer with less than a 24 month expected survival and/or cancer on active treatment with chemotherapy and/or radiation therapy. * Esophageal motility disorder, esophageal stricture or esophageal diverticulum, causing dysphagia or requiring dilatation. * GI obstruction or partial obstruction (by history or imaging), symptomatic GI stricture or pseudo-obstruction which may prevent passage of the capsule. * Patients with potentially reversible portal hypertension such as alcoholic hepatitis, acute viral hepatitis, untreated autoimmune hepatitis, or chronic hepatitis B or C on viral therapy.

Design outcomes

Primary

MeasureTime frame
The accuracy of capsule endoscopy for detecting esophageal varicesJune 2006-February 2008

Secondary

MeasureTime frame
Time to perform and interpret capsule endoscopy studyJune 2006-February 2008

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026