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N/A N=10

Cardiac Magnetic Resonance Imaging in Patients With Non-Hodgkin Lymphoma or Hodgkin Lymphoma Receiving Doxorubicin

Cardiac Toxicity · Chemotherapeutic Agent Toxicity · Lymphoma

Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Nov 2023
Primary outcome: Primary: Left Ventricular Ejection Fraction (LVEF) and Global Strain Decrease After Doxorubicin Chemotherapy — 5; 5 Participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
contrast-enhanced magnetic resonance imaging (Procedure)
Age
Adult, Older Adult · 19+ yrs
Sex
All
Sponsor
University of Nebraska
Primary completion
Mar 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Left Ventricular Ejection Fraction (LVEF) and Global Strain Decrease After Doxorubicin Chemotherapy
5; 5

Summary

RATIONALE: Diagnostic procedures, such as cardiac magnetic resonance imaging, may help doctors detect early changes in the heart caused by chemotherapy. PURPOSE: This clinical trial is studying how well cardiac magnetic resonance imaging works in patients with newly diagnosed non-Hodgkin lymphoma or Hodgkin lymphoma receiving doxorubicin.

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of non-Hodgkin lymphoma or Hodgkin lymphoma

o Newly diagnosed disease

  • Planning to receive doxorubicin hydrochloride-based chemotherapy solely at the University of Nebraska Medical Center
  • Fertile patients must use effective contraception
  • Able to lie flat for 90 minutes
  • Able to fulfill the requirements of the study

Exclusion Criteria

  • Not pregnant or nursing
  • No pacemaker
  • No chronic kidney disease stages 3-5 (glomerular filtration rate < 60 mL/min)
  • No metallic foreign body not approved for MRI
  • No known hypersensitivity to gadolinium contrast or other required drugs in the study
  • No comorbidity or condition which, in the opinion of the investigator, may interfere with the assessments and procedures of this study
  • No prior chemotherapy
  • No prior radiotherapy to mantle or mediastinum
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00577798). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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