Prognostic Factors of Acute Splenic Sequestration
NCT01207037 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 58
Last updated 2025-09-08
Summary
Acute splenic sequestration is a frequent and life threatening complication occurring in approximately 10 % of homozygous children. Maximal incidence is between 6 and 18 months.
The investigators formulate the hypothesis that there are clinical, biological and genetic markers predictive of severe complications notably acute splenic sequestration in SCD children. The present research project thus aims at analyzing in a forward-looking way the profile of severity by analysing clinical, biological and genetic characteristics in a multicentric cohort of 60 SCD children
Conditions
- Anemia; Drepanocytic
Interventions
- PROCEDURE
-
blood samples and scintigraphy
at 3 months, 6 months, 12 months, 18 months and 24 months will allow a clinical evaluation and an additional sampling of blood of 5 mL at each visit Scintigraphy at 6 months and 18 months
Sponsors & Collaborators
-
URC-CIC Paris Descartes Necker Cochin
collaborator OTHER -
Assistance Publique - Hôpitaux de Paris
lead OTHER
Principal Investigators
-
Valentine Brousse, MD, PhD · Assistance Publique - Hôpitaux de Paris
Study Design
- Allocation
- NA
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 3 Months
- Max Age
- 6 Months
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-08-12
- Primary Completion
- 2014-12-22
- Completion
- 2017-11-07
Countries
- France
Study Locations
More Related Trials
-
Prevention of Cerebral Infarction in Sickle Cell Anemia - Comprehensive Sickle Cell Center
NCT00005327 ·Status: COMPLETED
-
Sickle Cell Disease and Endothelial Progenitor Cells (EPCs)
NCT00783627 ·Status: COMPLETED
-
Metabolic and Hemodynamic Reserve in Pediatric SCA
NCT04406818 ·Status: RECRUITING ·Phase: NA
-
Pulmonary Hypertension, Hypoxia and Sickle Cell Disease
NCT00495638 ·Status: COMPLETED
-
Evaluation of the Lung Capillary Blood Volume in Children With Sickle Cell Disease
NCT00560261 ·Status: COMPLETED ·Phase: PHASE3
-
Role of Placenta Growth Factor in Sickle Acute Chest Syndrome
NCT00448370 ·Status: COMPLETED
-
Cooperative Assessment of Late Effects for SCD Curative Therapies
NCT05153967 ·Status: RECRUITING
-
SCRIPT: Sickle Cell Risk in Pregnancy Tool
NCT06529042 ·Status: ENROLLING_BY_INVITATION
-
Biological, Genetic and Environmental Involved in the Complications of Sickle Cell Disease
NCT04205123 ·Status: UNKNOWN
-
The Influence of micro-and Macro Vascular Dysfunction on Clinical Severity in Adults With Sickle Cell Anemia (SS) and Sickle Cell Hemoglobin C Disease (SC)
NCT07277023 ·Status: COMPLETED ·Phase: NA
-
Heart Arteries and Sickle Cell Disease / Coeur Artères DREpanocytose
NCT03114137 ·Status: UNKNOWN
-
Screening for Renal Complications in Children and Young Adults With Major Sickle Cell Disease
NCT05211037 ·Status: COMPLETED ·Phase: NA
-
Inflammation, Platelets and Sickle Cell Disease
NCT05646888 ·Status: ACTIVE_NOT_RECRUITING
-
Non Invasive Positive Pressure Ventilation for Prevention of Acute Chest Syndrome in Sickle Cell Disease
NCT01501643 ·Status: TERMINATED ·Phase: NA
-
Use of Macrolides in Acute Chest Syndrome: A Multicenter Retrospective Study
NCT07037706 ·Status: COMPLETED
-
Comparison of Patient Centered Outcomes for People With Sickle Cell Disease in the Acute Care Setting
NCT02411396 ·Status: COMPLETED
-
Lipid Balance in Adult Sickle Cell Patients
NCT05780775 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Cardiovascular Complications of Sickle Cell Disease
NCT01044901 ·Status: COMPLETED
-
Role of Inflammasome in Platelet Activation in Sickle Cell Disease Patient
NCT06986837 ·Status: COMPLETED
-
Study of Biological Markers in Children With Sickle Cell Disease
NCT04839159 ·Status: UNKNOWN ·Phase: NA
-
Study of a Deformability Parameter of Red Blood Cell
NCT05850156 ·Status: NOT_YET_RECRUITING
-
Prevalence and Pathophysiology of Systemic Arterial Pressure Abnormalities in Childhood Sickle Cell Disease
NCT04911049 ·Status: UNKNOWN
-
A 3-year, Prospective, Non-interventional, Multicenter Registry in Sickle Cell Disease (SCD) Patients
NCT01220115 ·Status: COMPLETED
-
HLA Haploidentical Bone Marrow Transplant in Patients With Severe Sickle Cell Disease
NCT03240731 ·Status: COMPLETED ·Phase: PHASE2
-
Hydroxyurea to Prevent Brain Injury in Sickle Cell Disease
NCT01389024 ·Status: COMPLETED ·Phase: PHASE2