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Enrolling by invitationNCT07181174Updated Sep 18, 2025

Early Prediction and Diagnosis of Acute Kidney Injury

An observational study in Early Diagnosis of Acute Kidney Injury, sponsored by Aswan University. Enrolling by invitation at 1 site in Egypt. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-09-18.

Sponsored by Aswan University · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as enrolling by invitation.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
45
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to estimate the accuracy of renal resistive index in early diagnosis and prediction of acute kidney injury in patients with hemorrhagic stroke. the main questions it aims to answer are :

  • Early detection of acute kidney injury in patient with hemorrhagic stroke .
  • Decrease morbidity and mortality rate in patients with hemorrhagic stroke .
02

Conditions studied

  • Early Diagnosis of Acute Kidney Injury
03

In context

Lead sponsor

Aswan University is the lead sponsor of 47 studies on the registry; 22 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

patients with hemorrhagic stroke

Inclusion criteria

All patients with hemorrhagic stroke presented to Aswan university hospital that will be fulfilled the following characters:

  • Age >18 years.
  • Both sex.
  • Cases of spontaneous onset

Exclusion criteria

Exclusion Criteria:

  • Age \< 18
  • Patients with traumatic hemorrhagic stroke.
  • Patients with brain tumors.
  • Patients with congenital anomalies of cerebral vessels e.g. AVM (arteriovenous malformation) and cerebral aneurysm.
  • Patients with history of any renal diseases
05

Study design

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

Interventions

  • DeviceUltrasonographic examination and doppler ultrasonography will be performed using a convex transducer.

    -Renal Resistive Index Measurement Method: Ultrasonographic examination and doppler ultrasonography will be performed using a convex transducer. First, the kidney is localised in the flanks with conventional B-mode ultrasonography, after which, color doppler images are acquired. The interlobar arteries were visualised, with the wavelength obtained by creating a 90-degree right-angle with the interlobar artery using a power doppler. After the manual determination of the peak systolic and end-diastolic velocities \* RRI will be calculated by the device using the formula: RRI = (peak systolic velocity - end-diastolic velocity) / (peak systolic velocity). RRI will be measured three times for each kidney and averaged

06

What researchers measure

Primary outcomes

  1. Early detection of acute kidney injury in patient with hemorrhagic stroke

    Time frame: within 2 days and 1 week

07

Study locations

1 site
  • Aswan university hospitals- Neurology Department
    Aswān, 1240801, Egypt
08

References and documents

Individual participant data

Plan to share: No

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 Sep 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07181174
Lead sponsor
Aswan University
Responsible party
Peter Essa (Resident of neuropsychiatry department, Aswan University) — Principal investigator
First posted
Sep 18, 2025
Start date
Dec 1, 2024
Primary completion
Dec 1, 2025 (estimated)
Completion
Jan 1, 2026 (estimated)
Last update
Sep 18, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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