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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00481416
Other study ID # MA-37
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 2004
Est. completion date January 2005

Study information

Verified date June 2006
Source Medtronic - MITG
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study is to access the accuracy of the PillCam Eso capsule in identifying the presence of suspected esophageal disease in patients undergoing surveillance or screening for esophageal disease by standard endoscopy


Description:

The procedure that is being evaluated in this study is an esophageal capsule which is part of the Given® Diagnostic System. This system has been developed for aiding the gastroenterologist in diagnosing small bowel diseases or disorders, as routine methods used today cannot explore the entire length of the small bowel in detail. It is currently available in more than 50 countries worldwide, including the Europe, USA, Canada, Central and South America, Australia and Asia. More than 300,000 capsules have already been ingested worldwide. In this study, a capsule developed and approved for the esophagus (food tube between the mouth and stomach) with two optical heads (mini cameras) will be used and intended to take better recorded pictures of the esophagus.

During the study the study participant will undergo a capsule endoscopy and an upper esophagoscopy. The method under investigation in this study is the capsule endoscopy.

The capsule endoscope is a small camera, about an inch long and less than half an inch wide, which you will be asked to swallow. The camera travels from a person's mouth all the way through their stomach and intestines and is eventually passed in the stool. The camera has a light source (like a flash on a regular camera) and takes pictures of the esophagus. The pictures are sent to a recorder, about the size of a wallet, using electronic signals for 20 minutes while the wireless endoscope goes through your esophagus. The disposable capsule is passed in the stool in an average of 24 hours.

After the capsule endoscopy the study participant will undergo the esophagoscopy. An esophagoscopy is the standard method used to view the esophagus. It involves inserting a long flexible tube with a light and camera on the end (called an endoscope) through the mouth and down the throat and esophagus. It may also involve the use of a sedative.

The study involves approximately two-three clinic visits.


Recruitment information / eligibility

Status Completed
Enrollment 318
Est. completion date January 2005
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Patient has prior endoscopic confirmation of esophageal varices and is undergoing surveillance endoscopy or

2. Patient has sign/symptoms of chronic liver disease, without previous diagnosis of esophageal varices,with clinical indication to undergo esophagoscopy (or EGD)

Exclusion Criteria:

1. Patient has difficulty swallowing

2. Patient has known Zenker's Diverticulum

3. Patient went through previous endoscopic treatment of esophageal varices

4. Patient is known or is suspected to suffer from intestinal obstruction

5. Patient has a cardiac pacemaker or other implanted electro medical device

6. Female patient is pregnant

7. Patient is expected to undergo MRI examination within 7 days after ingestion of the capsule

8. Patient has had a prior abdominal surgery of the gastrointestinal tract (other than uncomplicated appendectomy or uncomplicated cholecystectomy)

9. Patient has any condition, which precludes compliance with study and/or device instructions

10. Patient suffers from life threatening conditions

11. Patient is currently participating in another clinical study -

Study Design


Intervention

Device:
PillCam Eso


Locations

Country Name City State
Australia Royal Brisbane and Women's Hospital Herston Queensland
Israel Rambam Medical Center Haifa
United States Minnesota Gastroenterology Associates Plymouth Minnesota
United States Oregon Health Sciences University Portland Oregon
United States Mayo Clinic Hospital Scottsdale Arizona

Sponsors (2)

Lead Sponsor Collaborator
Medtronic - MITG Ethicon Endo-Surgery

Countries where clinical trial is conducted

United States,  Australia,  Israel, 

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Not yet recruiting NCT04254822 - HVPG-Guided Therapy vs Carvedilol Plus Endotherapy for the Prevention of Esophageal Variceal Rebleeding in Cirrhotic Patients N/A
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