ClinicalTrials.gg
Status unknownNCT03680547Updated Nov 29, 2019

Nephropathy in Patients With Sickle Cell Disease

An observational study in Sickle Cell Nephropathy, sponsored by Assiut University. Status unknown. Open to participants aged 5 Months to 18 Years. Per ClinicalTrials.gov, last updated 2019-11-29.

Sponsored by Assiut University · Observational

The sponsor has not verified this record recently (last verified Nov 2019), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
25
Ages
5 Months to 18 Years
Sex
All
01

Study summary

There are some diseases that give rise to diverse renal manifestations as does sickle cell disease

Read the detailed description

Such involvement adversely affects virtually all major physiological processes in the kidney, and leads to complications that are common and chronic on the one hand (such as impaired urinary concentrating ability), and those that are rare and uniformly fatal on the other (such as renal medullary carcinoma) This steady adverse renal sequelae shortens the average lifespan of patients with SCD.

Proteinuria and a reduced glomerular filtration rate are risk factors associated with increased mortality among those patients with approximately 16-18% of overall mortality in this patient group is due to kidney disease.

Once end stage renal disease is reached, the mortality of patients who are on haemodialysis and have SCD is increased severalfold relative to the mortality of patients who are on haemodialysis but do not have SCD.

Thus,although the average lifespan of patients with SCD has increased during recent decades owing to improved management of complications outside the kidney,kidney disease contributes substantially to the still increased mortality in SCD.

02

Conditions studied

  • Sickle Cell Nephropathy
03

In context

Lead sponsor

Assiut University is the lead sponsor of 5,050 studies on the registry; 2,174 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Months to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

to assess degree of renal affection in patients with sickle cell disease attending Assuit university Children hospital by estimating some predictors of glomerular and tubular dysfunction.detailed history taking and thorough clinical examination and laboratory investigations

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All patients with sickle cell anemia attending the unit will be included in the study.

Exclusion criteria

Exclusion Criteria:

  • patient with any underlaying systemic diseases other than sickle cell anaemia
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
25 participants (estimated)
Patient registry
No

Interventions

  • Otherpatient with sickle cell disease

    assess degree of renal affection in patientswith sickle cell disease attending Assuit university Children hospital by estimating some predictors of glomerular and tubular dysfunction.

06

What researchers measure

Primary outcomes

  1. sickle cell nephropathy in patient with sickle cell disease

    detection of renal impairment in patients with sickle cell disease by estamating gloerular and tubular dysfunction clinicaly and laboratory

    Time frame: one year

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 29, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03680547
Lead sponsor
Assiut University
Responsible party
omnia talat hasan (assiut, Assiut University) — Principal investigator
First posted
Sep 21, 2018
Start date
May 1, 2020 (estimated)
Primary completion
May 30, 2020 (estimated)
Completion
Jan 1, 2021 (estimated)
Last update
Nov 29, 2019

Study contacts

fahim mohamed fahim
Contact
fahim.osman@med.aun.edu.eg
01002500073
ahlam badawi ali
Contact
ahlam.badawi@med.aun.edu.eg
01006807866
omnia talat hasan
principal investigator · assiut

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2019. You cannot join it, but the record below documents what was studied.

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