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Cystatin c: a Biomarker of AKI in Aneurysmal Subarachnoid Haemorrhage Patients

A

Alexandria University

Status

Completed

Conditions

Acute Kidney Injury

Treatments

Diagnostic Test: cystatin c

Study type

Observational

Funder types

Other

Identifiers

NCT06635408
9222704

Details and patient eligibility

About

The goal of this observational study is to assess cystatin c as a predictive biomarker of early acute kidney injury in aneurysmal subarachnoid hemorrhage patients. The main question it aims to answer is:

  • Does cystatin c biomarker can predict early acute kidney injury in aneurysmal subarachnoid hemorrhage patients?

Participants will be grouped into Aki and Non-Aki groups based on RIFLE criteria and Cystatin c biomarker will be tested to answer the study question.

Enrollment

52 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patient admission to hospital within 48 hours of subarachnoid haemorrhage onset.
  • Subarachnoid haemorrhage caused by intracranial aneurysm rupture and is confirmed via computed tomography angiography (CTA).
  • Medical treatment, microsurgical clipping, or interventional endovascular treatment of aneurysm is performed within 48 hours of subarachnoid haemorrhage onset.

Exclusion criteria

  • Prior onset of subarachnoid haemorrhage or other neurological diseases such as ischemic stroke, hemorrhagic stroke, or severe head trauma.
  • Systemic diseases, such as chronic liver diseases, chronic lung diseases, chronic heart failure, thyroid diseases and cancer.
  • Renal impairment at time of admission (creatinine-based eGFR less than 60 ml/min per 1.73 m2 body surface area).
  • Patients who are hemodynamically unstable at time of admission.
  • Mortality within 10 days after admission (duration of study).

Trial design

52 participants in 2 patient groups

Aki group
Description:
Cystatin c biomarker will be assessed to predict occurrence of early acute kidney injury
Treatment:
Diagnostic Test: cystatin c
Non-Aki group
Description:
participants in this group will not develop acute kidney injury throughout the study duration
Treatment:
Diagnostic Test: cystatin c

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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