World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 8 August 2016
Main ID:  NCT02394431
Date of registration: 10/03/2015
Prospective Registration: No
Primary sponsor: Brugmann University Hospital
Public title: Added Value of Speckle Tracking in the Evaluation of Patients With Sickle Cell Disease
Scientific title: Added Value of Speckle Tracking in the Evaluation of Patients With Sickle Cell Disease
Date of first enrolment: November 2013
Target sample size: 62
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02394431
Study type:  Observational
Study design:  Observational Model: Cohort, Time Perspective: Prospective  
Phase:  N/A
Countries of recruitment
Belgium
Contacts
Name:     Marielle MORISSENS, MD
Address: 
Telephone:
Email:
Affiliation:  CHU Brugmann
Key inclusion & exclusion criteria

Inclusion Criteria:

- All sickle cell disease patients

Exclusion Criteria:

- Insufficient echogenicity



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Sickle Cell Disease
Intervention(s)
Other: Biological parameters
Other: Cardiac echography
Other: Clinical parameters
Primary Outcome(s)
Cardiac diastolic function [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Cardiac ejection fraction [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Global longitudinal strain [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
arterial pulmonary hypertension [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Cardiac tissular doppler [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
left ventricular hypertrophy [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Myocardiac performance index [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Secondary Outcome(s)
Biological parameters: red cells count [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Clinical parameters: severity of the illness [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Biological parameters: ferritin levels [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Biological parameters: hematocrit levels [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Biological parameters: hemoglobin levels [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Clinical parameters: sanguine transfusion numbers [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Biological parameters: iron levels [Time Frame: once per year, at the annual medical visit planned according to the standart of care for this pathology]
Secondary ID(s)
CHUB-Echo-Cardio
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history