Evaluation of PillCam® Express Capsule Endoscopy Delivery System

NCT ID: NCT01088646

Last Updated: 2020-10-22

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 25 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-10-31
• Study Completion Date: 2010-05-31

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of a trans-endoscopic capsule placement Capsule Endoscopy Delivery System.

Detailed Description

Natural ingestion of a wireless capsule endoscope (e.g. PillCam™ SB) is contraindicated in subjects with oropharyngeal or mechanical dysphagia, gastroparesis and known or suspected anatomical abnormalities. In addition, ingestion of a wireless capsule endoscope may be challenging in the pediatric population. The PillCam® Express Capsule Endoscopy Delivery System is intended to provide physicians with the capability to place capsules in the proximal duodenum using the accessory channel of a standard endoscope.

The PillCam™ SB capsule to be used in this study was cleared by the FDA in August 2001 for small bowel evaluation. It has been ingested to date by more than 1,000,000 people worldwide and is well accepted by subjects and physicians as well as the professional societies.

Further details of the PillCam®Express Capsule Endoscopy Delivery System can be found in the device description section.

This study is designed to evaluate the performance and safety of the Capsule Endoscopy Delivery System in subjects indicated to undergo a standard Esophagogastroduodenoscopy (EGD) endoscopy

Conditions

Small Bowel Disease; Inflammatory Bowel Disease

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DEVICE_FEASIBILITY
• Blinding Strategy: SINGLE

Interventions

PillCam® Express Capsule Endoscopy Delivery System

The PillCam® Express Capsule Endoscopy Delivery System is comprised of three parts: a catheter, a syringe and the capsule holder. The catheter is passed through the accessory channel of a standard endoscope and the capsule holder is snapped on to the distal end of the device. The endoscope is used to guide the Capsule Endoscopy Delivery System to the proximal duodenum. The capsule is then released pneumatically, using an air-filled syringe attached to the proximal end of the catheter.

Once the capsule is deployed, the endoscope is withdrawn and the capsule holder is cut off at the distal part of the device with scissors. The catheter is then retracted and discarded.

The PillCam® Express Capsule Endoscopy Delivery System is single-use, disposable and latex-free.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Age ≥ 2 years
• Subject scheduled for EGD endoscopy with a 2.8 mm (or greater) working channel

Exclusion Criteria

• Subject is known or is suspected to suffer from bowel obstruction or bowel perforation at the time of presentation
• Subject has history of UGI tract surgery (e.g., Billroth I, Billroth II, esophagectomy, gastrectomy, bariatric procedure)
• Presence of an electro-medical device (pacemaker or internal cardiac defibrillator)
• Subject is pregnant
• Subject is expected to undergo a MRI examination within 7 days after ingestion of the capsule
• Subject has known allergy to conscious sedation medications
• Subject or legal guardian is not able to provide written informed consent

• Minimum Eligible Age: 2 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Medtronic - MITG

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jonathan Leighton, MD

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Peter Legnani, MD

Role: PRINCIPAL_INVESTIGATOR

Private Practice New York, New York

Locations

Alabama Digestive Disorders Center, P. C.

Huntsville, Alabama, United States

Alabama Liver and Digestive Specialists

Montgomery, Alabama, United States

RANY -Research Associates of New York (NY Gastroenterology Associates)

New York, New York, United States

Countries

United States

Other Identifiers

RD-300

Identifier Type: -

Identifier Source: org_study_id