Anemia, Sickle Cell Clinical Trial
Official title:
Comprehensive Sickle Cell Centers Collaborative Data Project (C-Data)
Sickle cell disease (SCD), also known as sickle cell anemia, is an inherited blood disease that can cause intense pain episodes. The purpose of this study is to gather medical information from children and adults with SCD and establish a database so that researchers can contact people to participate in future SCD research studies.
SCD is an inherited blood disorder. Symptoms include anemia, infections, organ damage, and
intense episodes of pain, which are called "sickle cell crises." The Comprehensive Sickle
Cell Centers (CSCC) is a network of 10 centers that conduct research to improve health care
and treatment options for people with SCD. This study, the Collaborative Data Project
(C-Data), will establish a comprehensive database of children and adults receiving medical
care at participating CSCC research centers who are potentially eligible for inclusion in
SCD clinical trials. The main purposes of this study are the following: 1) to gather medical
information about a large number of people with SCD over a long period of time; 2) to
identify potential participants for future SCD clinical trials; 3) to collect information
about how SCD affects quality of life; and 4) to evaluate the relationship between SCD
patients' characteristics and medical events.
In this study, research staff will review participants' medical records twice a year for at
least 5 years. Information will be collected regarding participants' medical history,
physical exams, blood tests, and demographics. Once a year, participants will take part in a
short interview about their health and lifestyle. Participants will also complete
quality-of-life and patient satisfaction questionnaires during the first year of the study
and may complete additional questionnaires in the future. During an interview, participants
will be asked general questions about their experience with SCD and more specific questions
on headaches and any possible relation they may have to SCD pain. Participants may also be
asked to provide a blood sample at some point during the study. CSCC researchers will
analyze the information in the database and may contact participants in the future to see if
they are interested in enrolling in SCD clinical trials.
;
Observational Model: Cohort
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06078696 -
Siplizumab for Sickle Cell Disease Transplant
|
Phase 1/Phase 2 | |
Completed |
NCT04134299 -
To Assess Safety, Tolerability and Physiological Effects on Structure and Function of AXA4010 in Subjects With Sickle Cell Disease
|
N/A | |
Completed |
NCT02561312 -
Comparison of Two Methods of Transfusion for Stroke Prevention in Sickle Cell
|
||
Completed |
NCT00890396 -
Long-Term Effects of Hydroxyurea in Children With Sickle Cell Anemia (The BABY HUG Follow-up Study)
|
||
Completed |
NCT00059293 -
Transcranial Doppler (TCD) Ultrasound of Subjects Enrolled in BABY HUG - Ancillary to BABY HUG
|
||
Terminated |
NCT00034528 -
Stem Cell Transplantation After Reduced-Dose Chemotherapy for Patients With Sickle Cell Disease or Thalassemia
|
Phase 2 | |
Completed |
NCT00005277 -
Cooperative Study of The Clinical Course of Sickle Cell Disease
|
N/A | |
Active, not recruiting |
NCT04170348 -
Daily Vitamin D for Sickle-cell Respiratory Complications
|
Phase 2 | |
Completed |
NCT04584528 -
Implementing an Individualized Pain Plan (IPP) for ED Treatment of VOE's in Sickle Cell Disease
|
N/A | |
Recruiting |
NCT02286154 -
Therapeutic Response Evaluation and Adherence Trial (TREAT)
|
N/A | |
Completed |
NCT02857023 -
Feasibility and Efficacy of a Home-based, Computerized Cognitive Training Program in Pediatric Sickle Cell Disease
|
N/A | |
Withdrawn |
NCT01925001 -
Phase 2 Study of MP4CO to Treat Vaso-occlusive Sickle Crisis
|
Phase 2 | |
Terminated |
NCT00122980 -
Stroke With Transfusions Changing to Hydroxyurea
|
Phase 3 | |
Completed |
NCT00246077 -
Quality of Life of Children With Sickle Cell Disease Who Are Getting Chronic Transfusions With a Lifeport
|
N/A | |
Completed |
NCT00094887 -
Nitric Oxide Inhalation to Treat Sickle Cell Pain Crises
|
Phase 2 | |
Completed |
NCT00035763 -
Pain in Sickle Cell Epidemiologic Study
|
N/A | |
Terminated |
NCT04091737 -
CSL200 Gene Therapy in Adults With Severe Sickle Cell Disease
|
Phase 1 | |
Completed |
NCT00005300 -
Investigation of Selected Patient Groups From The Cooperative Study of Sickle Cell Disease
|
N/A | |
Recruiting |
NCT04351698 -
SMILES: Study of Montelukast in Sickle Cell Disease
|
Phase 2/Phase 3 | |
Not yet recruiting |
NCT06290401 -
A Socio-ecological Approach for Improving Self-management in Adolescents With SCD
|
Phase 2 |