Development of Applications of the ® PillCam Endoscopy System and Evaluation of Their Performance

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02775708

Acronym

NOISE

Enrollment

Registered

2016-05-18

Start date

2016-03-31

Completion date

2017-10-24

Last updated

2017-11-01

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

Conditions

Any Gastric Condition Which Requires Capsule Endoscopy

Brief summary

The purpose of this study is to support development of PillCam Endoscopy System applications.

Interventions

DEVICEPillcam endoscopy system

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

OTHER

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Subject's from 18 years of age. * Subject is indicated for Capsule Endoscopy procedure. * Subject agrees to sign the Informed Consent Form.

Exclusion criteria

* Female subject is pregnant. * Subject is known or is suspected to suffer from intestinal obstruction (symptoms such as severe abdominal pain with accompanying nausea or vomiting). * Subject has a pacemaker or other implanted electro-medical device. * Subject has any condition, which precludes compliance with study and/or device instructions, such as swallowing problems. * Subject suffers from life threatening conditions. * Subject is currently participating in another clinical study that may directly or indirectly affect the results of this study

Design outcomes

Primary

Measure	Time frame
Number of gaps in the RAPID video will be assessed	capsule endoscopy procedure day

Countries

Germany, Spain

Outcome results

None listed

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