Diastolic Dysfunction in Sickle Cell Disease During Vaso-occlusive Crisis
This study is currently recruiting participants.
Verified September 2012 by King Abdullah International Medical Research Center
Sponsor:
King Abdullah International Medical Research Center
Collaborator:
King Abdulaziz Medical City
Information provided by (Responsible Party):
Abdulsalam Alaithan, King Abdulaziz Medical City
ClinicalTrials.gov Identifier:
NCT01683968
First received: September 8, 2012
Last updated: September 12, 2012
Last verified: September 2012
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Purpose
This study is designed to investigate the presence and absence of abnormal heart muscle contractions during sickle cell crises.
You will be asked to do echocardiography during and after your admission to the hospital. We will compare tow pictures and study the differences.
| Condition |
|---|
|
Sickle Cell |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Diastolic Dysfunction in Sickle Cell Disease During Vaso-occlusive Crisis |
Resource links provided by NLM:
Genetics Home Reference related topics:
sickle cell disease
MedlinePlus related topics:
Sickle Cell Anemia
U.S. FDA Resources
Further study details as provided by King Abdullah International Medical Research Center:
| Estimated Enrollment: | 216 |
| Study Start Date: | September 2012 |
| Estimated Study Completion Date: | October 2015 |
| Estimated Primary Completion Date: | October 2015 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
Sickle cell
Patient who are admitted with sickle cell crises
|
Show Detailed Description Eligibility| Ages Eligible for Study: | 14 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Adult patient admitted to the hospital with vaso-occlusive crisis
Criteria
Inclusion criteria:
- Patients older than 18 years
- Diagnosis of acute vaso-occlusive crisis due to sickle cell disease.
- Informed consent
Exclusion criteria:
- Congenital heart disease
- Long standing hypertension
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01683968
Contacts
| Contact: Dr Abdulsalam M Alaithan, MD | 96635910000 ext 33445 | aithana@ngha.med.sa |
Locations
| Saudi Arabia | |
| King Abdulaziz Hospital | Recruiting |
| Al-Ahsa, EP, Saudi Arabia, 31982 | |
| Contact: Abdulsalam MA Alaithan, MD 96635910000 ext 33445 aithana@ngha.med.sa | |
Sponsors and Collaborators
King Abdullah International Medical Research Center
King Abdulaziz Medical City
More Information
No publications provided
| Responsible Party: | Abdulsalam Alaithan, CONSULTANT INTENSIVEST AND PULMONOLOGIST, King Abdulaziz Medical City |
| ClinicalTrials.gov Identifier: | NCT01683968 History of Changes |
| Other Study ID Numbers: | RE11/027 |
| Study First Received: | September 8, 2012 |
| Last Updated: | September 12, 2012 |
| Health Authority: | Saudi Arabia: Ethics Committee |
Additional relevant MeSH terms:
|
Anemia, Sickle Cell Anemia, Hemolytic, Congenital Anemia, Hemolytic Anemia |
Hematologic Diseases Hemoglobinopathies Genetic Diseases, Inborn |
ClinicalTrials.gov processed this record on May 22, 2013