Flavoring Oral Contrast for MR Enterography

NCT ID: NCT02617576

Last Updated: 2017-01-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2016-01-31

Study Completion Date

2016-12-31

Brief Summary

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To determine if patient satisfaction, participation, and image quality improves with flavored oral contrast for MR enterography.

Detailed Description

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Volumen is an oral contrast agent used in MR imaging of the bowel. It has an unpleasant taste which makes it difficult for pediatric patients, especially sick pediatric patients, to drink. There are other contrast materials used in the department that are flavored to improved patient participation. The investigators hope to determine a way to flavor Volumen to improve patient participation. In doing so, the investigators hope to also improve patient satisfaction as well as imaging quality.

Conditions

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Taste, Altered

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Flavored contrast

This group of patients will have the choice to flavor their contrast.

No interventions assigned to this group

Unflavored contrast

This group of patients will drink the contrast without flavoring.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* pediatric patients having a MR enterography

Exclusion Criteria

* sedated patients
Minimum Eligible Age

8 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Minnesota

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Kelly Dietz, MD

Role: PRINCIPAL_INVESTIGATOR

University of Minnesota

Other Identifiers

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1507M76622

Identifier Type: -

Identifier Source: org_study_id

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