NCT07181174

Brief 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 .

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
45

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 2024

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2024

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

September 12, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 18, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2026

Completed
Last Updated

September 18, 2025

Status Verified

August 1, 2025

Enrollment Period

1 year

First QC Date

September 12, 2025

Last Update Submit

September 17, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Early detection of acute kidney injury in patient with hemorrhagic stroke

    within 2 days and 1 week

Interventions

-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

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

patients with hemorrhagic stroke

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Aswan university hospitals- Neurology Department

Aswān, 1240801, Egypt

Location

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident of neuropsychiatry department

Study Record Dates

First Submitted

September 12, 2025

First Posted

September 18, 2025

Study Start

December 1, 2024

Primary Completion

December 1, 2025

Study Completion

January 1, 2026

Last Updated

September 18, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations