FindTrial
Sign In

Prevalence Of Microalbuminuria Among Children Suffering From Sickle Cell Nephropathy and Sickle Cell/Beta-Thalassemia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01092169
Enrollment
Unknown
Registered
2010-03-24
Start date
Unknown
Completion date
Unknown
Last updated
2010-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Beta-Thalassemia, Microalbuminuria, Sickle Cell Anemia

Brief summary

Sickle cell nephropathy is a known complication of sickle cell anemia (SCA) manifested by increase in glomerular filtration rate (glomerular hyperfiltration) and results in proteinuria and chronic renal failure. Our goal is to examine the prevalence of proteinuria and microalbuminuria as an early predictive factor of glomerular injury, among young people who suffer from SCA as well as those who suffer from combined sickle cell/beta-thalassemia.

Interventions

OTHERNo intervention

Sponsors

Hillel Yaffe Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
No minimum to 25 Years
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with sickle cell anemia * Patients diagnosed with combined sickle cell anemia/beta-thalassemia

Exclusion criteria

* Diabetes mellitus * Hypertension * Reduced renal mass (single kidney) * Overweight * History of UTIs

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026