RECRUITING

Sickle Cell Kidney Biorepository

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Kidney disease is a major cause of illness and death in people with sickle cell disease and sickle cell trait. Despite these concerning facts, we do not (1) have an in-depth understanding of how kidney disease starts in sickle cell disease and sickle cell trait, (2) have detailed insights into why kidney disease is worse in people with sickle cell disease and sickle cell trait, (3) have management options that are tailored to treating or preventing kidney disease in people with sickle cell disease or sickle cell trait. The SCeK Biorepository is a specialized, secure repository designed for the collection of blood and urine samples from people with sickle cell disease and sickle cell trait. These samples are connected to detailed medical records, with the sole purpose of allowing researchers to better understand how kidney disease starts and progresses in people with the sickle cell gene. By studying these stored samples (using new tests) together with health information, researchers can find better early warning signs of kidney injury and develop better ways to protect kidney health in people with sickle cell disease and sickle cell trait.

Official Title

Sickle Cell Kidney (SCeK) Biorepository

Quick Facts

Study Start:2024-08-22
Study Completion:2049-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07064174

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age over 18 years,
  2. 2. Estimated glomerular filtration rate greater than or equal to 15 mL/min,
  3. 3. Presence of any hemoglobinopathy (will need to be confirmed by hemoglobin electrophoresis or genetic testing),
  4. 4. Controls (absence of hemoglobinopathy) will be subject to review and only selected if demographics are identical to a currently enrolled participant with a hemoglobinopathy.
  1. 1. Age 66 years or older,
  2. 2. Estimated glomerular filtration rate less than 15 mL/min or on dialysis,
  3. 3. Active pregnancy (may be enrolled 4 weeks or more after delivery),
  4. 4. Active sickle cell pain episode requiring hospitalization or emergency room visit or pain infusion clinic visit (may be enrolled 2 weeks or more after resolution of severe pain),
  5. 5. Active malignancy on induction or consolidation treatment. Maintenance chemotherapy in remission will be considered,
  6. 6. Prisoners.

Contacts and Locations

Study Contact

Kabir O Olaniran, MD, MPH, FASN
CONTACT
214-645-8267
SCeK@UTSouthwestern.edu

Study Locations (Sites)

Parkland Memorial Hospital
Dallas, Texas, 75235
United States
University of Texas Southwestern Medical Center
Dallas, Texas, 75390
United States

Collaborators and Investigators

Sponsor: University of Texas Southwestern Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-08-22
Study Completion Date2049-12

Study Record Updates

Study Start Date2024-08-22
Study Completion Date2049-12

Terms related to this study

Additional Relevant MeSH Terms

  • Sickle Cell Trait
  • Sickle Cell Disease (SCD)
  • Chronic Kidney Disease