Intra-individual Open-label, Single Center Study to Compare Unenhanced MRI With Dotarem Enhanced MRI

NCT ID: NCT03023566

Last Updated: 2022-05-20

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 250 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2017-02-09
• Study Completion Date: 2017-11-12

Brief Summary

The goal of this study is to evaluate safety and efficacy of Dotarem enhanced MRI in pediatric and neonatal population who are referred for contrast enhanced MRI at Phoenix Children's Hospital.

Detailed Description

Phoenix Children's Hospital (PCH) performs approximately 200 contrast enhanced MRI procedures per month. Recently PCH changed its MRI contrast agent from the linear contrast agent Magnevist to the macrocyclic contrast agent Dotarem. The goal of this study is to evaluate safety and efficacy of Dotarem enhanced MRI in pediatric and neonatal population who are referred for contrast enhanced MRI at PCH.

The study is designed as a single center, open label comparison of unenhanced MRI with Dotarem enhanced MRI in pediatric patient population (<18years). The comparison will be performed intra-individually by 3 independent blinded radiologists. Overall, the study population will consist of 250 pediatric patients who are indicated for contrast enhanced MRI. The safety follow-up period will be 24 (+/- 4) hours post injection of Dotarem and includes the assessment of physical examinations and vital signs as well as the assessment of AEs.

Conditions

Brain Diseases

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Dotarem Enhanced MRI

All pediatric patients (\< 18 years) scheduled for clinically indicated contrast enhanced MRI (Brain MRI with/without contrast) will receive a single IV bolus injection of Dotarem at a dose of 0.1 mmol/kg bw at a flow rate of 1-2 mL/sec followed by saline flush (routine/ standard of care).

Dotarem

Intervention Type: DRUG

Dotarem at dose of 0.1 mmol/kg of body weight (routine/standard of care)

Interventions

Dotarem

Dotarem at dose of 0.1 mmol/kg of body weight (routine/standard of care)

Intervention Type: DRUG

Other Intervention Names

gadoterate meglumine

Eligibility Criteria

Inclusion Criteria

• Any patient under 18 years of age who is scheduled for contrast enhanced MRI examination as part of their standard of care.
• Patients who are willing to undergo contrast enhanced MRI procedure
• Patients who are willing to comply with the study procedures (e.g. being followed-up for 24 hours after MRI procedure).
• Patients who have given their fully informed and written consent voluntarily.

Exclusion Criteria

• Patients receiving an MRI exam without contrast.
• Patients who are pregnant, lactating or who are > 11 years old and have not had a negative urine pregnancy test the same day as administration of Dotarem. The manufacturer's instructions for performing the urinary pregnancy test are to be followed.
• Having an underlying disease or concomitant medication which may interfere with efficacy or safety evaluations as planned in this study.
• Patients with a Glomerular Filtration Rate (GFR) < 30.
• Having received any investigational drug within 30 days prior to entering this study or who are planned to receive any investigational drug during the 24 (+ / - 4) hour safety follow-up period.
• Not being able to remain lying down for at least 45 - 60 min (e.g. patients with unstable angina, dyspnea at rest, severe pain at rest, severe back pain).
• Presenting with history of anaphylactoid or anaphylactic reaction to any allergen including drugs and contrast agents .
• Patients who have received any other contrast medium within 24 hours prior to Dotarem injection or are scheduled to receive any other contrast medium within the follow-up period.
• Being clinically unstable and whose clinical course during the 24 (+ / - 4) hours observation period is unpredictable.
• Being scheduled for, or likely to require, any surgical intervention within 24 hours before or within the follow-up period.
• Having any contraindication to MRI examination (e.g. pacemaker, recent wound clips, and severe claustrophobia).
• Having been previously enrolled in this study.

• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Guerbet

INDUSTRY

Sponsor Role: collaborator

Phoenix Children's Hospital

OTHER

Sponsor Role: lead

Responsible Party

Jeffrey Miller, MD

Staff Physician, Vice Chair of Radiology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jeffrey H Miller, MD

Role: PRINCIPAL_INVESTIGATOR

Phoenix Children's Hospital

Locations

Phoenix Children's Hospital

Phoenix, Arizona, United States

Countries

United States

Other Identifiers

PCH IRB#16-102

Identifier Type: -

Identifier Source: org_study_id