Study of Ventilatory Mechanics in Patients With Sickle Cell Anemia
NCT02565849 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 80
Last updated 2015-10-01
Summary
The Sickle Cell Anemia (SCA) is a recessive genetic condition, monogenic, resulting in defects in the red cell structure. In the investigators' country, this disease affects about 3,000 children each year and is considered one of the most prevalent disorders among the group of existing hereditary diseases.
The lungs are frequently affected in this disease by Acute Chest Syndrome (STA). Besides being the leading cause of death and the second leading cause of hospitalization in SCA, the STA is correlated with cognitive impairment frame these patients, resulting secondary Stroke vaso-occlusion of capillaries that supply the brain tissue.
Traditional tests of pulmonary function allow assess whether the person has any commitment in the respiratory system, whether obstructive, restrictive or mixed. To run these tests it is necessary that the patient understands and performs a forced expiratory maneuver to obtain reliable results. In the particular case of SCA, performing these tests it is very difficult due to the presence of cognitive impairment of varying degrees. This results in underdiagnosis of early changes in the lung parenchyma during the therapeutic window, committing the proper monitoring and treatment offered to these patients.
Conditions
Sponsors & Collaborators
-
Rio de Janeiro State University
lead OTHER
Principal Investigators
-
Cirlene Marinho · University Hospital Pedro Ernesto
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2013-02-28
- Primary Completion
- 2015-07-31
- Completion
- 2015-08-31
More Related Trials
-
Heart Disease in Sickle Cell Anemia
NCT00113152 ·Status: COMPLETED
-
Evaluation of Therapeutic Adherence to Inciting Spirometry in Sickle Cell Patients
NCT04667325 ·Status: COMPLETED
-
Longitudinal Changes in Exercise Capacity in Children and Young Adults With Sickle Cell Anemia
NCT01558076 ·Status: COMPLETED
-
Motivations, Expectations, and Decision-making of Sickle Cell Patients in Clinical Research
NCT03709303 ·Status: COMPLETED
-
VO2max & HRQoL in Children With Sickle Cell Disease
NCT05995743 ·Status: COMPLETED
-
Pulmonary Hypertension, Hypoxia and Sickle Cell Disease
NCT00495638 ·Status: COMPLETED
-
Carbon Monoxide Levels and Sickle Cell Disease Severity
NCT01547793 ·Status: COMPLETED
-
Long-term Endurance Training in Sickle Cell Disease Patients: Impact on Clinical Profile, Physical Fitness, and Quality of Life.
NCT06823219 ·Status: RECRUITING ·Phase: NA
-
Autonomic Nervous System and Sickle Cell Disease
NCT04062409 ·Status: COMPLETED
-
Exercise Capacity in Pediatric Sickle Cell Anemia
NCT01527799 ·Status: COMPLETED
-
Prevention of Cerebral Infarction in Sickle Cell Anemia - Comprehensive Sickle Cell Center
NCT00005327 ·Status: COMPLETED
-
Hemostasis in Sickle Cell Disease--Infancy to Adulthood
NCT00005703 ·Status: COMPLETED
-
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
-
Qualitative Survey of Potential Exercise Activity in Adults With Sickle Cell Anemia (SCA)
NCT04181944 ·Status: COMPLETED ·Phase: NA
-
Evaluation of the Hemostatic Potential in Sickle Cell Disease Patients
NCT02565082 ·Status: COMPLETED ·Phase: NA
-
Risk-based Therapy for Sickle Cell Anemia: A Feasibility Study
NCT02090296 ·Status: WITHDRAWN ·Phase: PHASE2
-
Exploring Near Infrared Spectroscopy (NIRS) Technologies for Assessment of Muscle Physiology, Tissue Oxygenation, and Blood Flow in Patients With Sickle Cell Disease (SCD)
NCT05604547 ·Status: COMPLETED
-
Sleep Study in Adult Patients With Major Sickle Cell Disease With Paroxysmal Nocturnal Events
NCT02539771 ·Status: COMPLETED ·Phase: NA
-
Pathophysiology of Acute Pain in Patients With Sickle Cell Disease
NCT03049475 ·Status: COMPLETED
-
Venous Thrombosis Biomarkers in Sickle Cell Disease and Sickle Cell Trait
NCT04349189 ·Status: COMPLETED
-
Exploration of the Parameters Influencing the Effort Limitation of Patients Suffering From Homozygous Sickle Cell Anemia
NCT06743139 ·Status: COMPLETED
-
Hemoglobin Desaturation in Sickle Cell Disease
NCT03908385 ·Status: COMPLETED
-
Metabolic and Hemodynamic Reserve in Pediatric SCA
NCT04406818 ·Status: RECRUITING ·Phase: NA
-
Implication of the Oxydative Stress in the Pathophysiology of Sickle Cell Anemia:
NCT03368924 ·Status: COMPLETED ·Phase: NA
-
State Of The Art Functional Imaging In Sickle Cell Disease
NCT01137721 ·Status: COMPLETED