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Not yet recruitingNCT06628700Updated Oct 8, 2024

Burden Fatty Liver Among Acute Ischemic Cerebral Stroke Patients

An observational study in Fatty Liver and Acute Ischemic Cerebral Stroke, sponsored by Assiut University. Not yet recruiting. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2024-10-08.

Sponsored by Assiut University · Observational

From the registry’s dates

  • Primary completion was expected by Oct 2025, 11 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
97
Ages
18 Years to 60 Years
Sex
All
01

Study summary

  1. Assess frequency of hepatic steatosis among patients in patients with Ischemic stroke without previous risk factors
  2. Assess outcomes morbidity and mortality ischemic stroke in correlation with hepatic steatosis .
Read the detailed description

Fatty liver disease, encompassing both alcoholic and non-alcoholic variants, is a growing health concern worldwide, with prevalence rates soaring in parallel with obesity and diabetes epidemics. The estimated global incidence of NAFLD alone is 47 cases per 1,000 people, with a higher rate observed in males than females. Among adults worldwide, the estimated prevalence of NAFLD is 32%, with a higher prevalence in males (40%) compared to females (26%), making it the most common liver disorder. The hazards of fatty liver disease extend beyond the liver itself .The condition is characterized by the accumulation of excess fat in liver cells, which can progress to more severe liver diseases, such as steatohepatitis, fibrosis, cirrhosis, and hepatocellular carcinoma.

Early assessment and diagnosis of liver steatosis are crucial for managing and mitigating the risks associated with FLD. Non-invasive methods, such as elastography combined with the Controlled Attenuation Parameter (CAP) score, have emerged as effective tools for detecting and quantifying liver fat content. These methods offer a less invasive alternative to liver biopsies, providing reliable data to guide clinical decisions.

NAFLD is characterized by a proinflammatory and proatherogenic state that causes vascular inflammation and neurodegeneration, potentially leading to both clinical and subclinical cerebrovascular disease. Increasing epidemiological evidence links NAFLD to a higher risk and greater severity of stroke, independent of other vascular risk factors.Additionally, studies suggest NAFLD is involved in subclinical cerebrovascular diseases, such as carotid atherosclerosis which is characterized by the build-up of plaques in the carotid arteries. Patients with NAFLD exhibited greater carotid atherosclerosis .

02

Conditions studied

  • Fatty Liver
  • Acute Ischemic Cerebral Stroke

Keywords

  • Fatty liver
  • Acute ischemic cerebral stroke
  • Hepatic steatosis
03

In context

Fatty Liver

1,451 studies on the registry are indexed under Fatty Liver; 292 are open to participants now.

This study's planned enrollment of 97 is below the median of 140 across 397 observational studies indexed under Fatty Liver.

Browse Fatty Liver studies →

Lead sponsor

Assiut University is the lead sponsor of 4,901 studies on the registry; 2,098 are open to participants now.

Of its 13 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
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Newly diagnosed ischemic cerebral stroke patients exceeding of window phase without obvious risk factors.

Inclusion criteria

  • Newly diagnosed ischemic cerebral stroke exceeding of window phase without obvious risk factors.
  • patients above 18 years.
  • patients below 60 years.

Exclusion criteria

Exclusion Criteria:

  • patients have obvious risk factors including: smoking, DM , Hypertension ,renal patients , cardiovascular diseases (AF , valvular disease ,reduced systolic function ,chronic HCV ,HBV).
  • patients below 18 years.
  • patients above 60 years.
  • patients refused to contribute to this study.
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
97 participants (estimated)
Target follow-up
20 Days
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. Assess frequency of hepatic steatosis among patients in patients with Ischemic stroke without previous risk factors

    Time frame: Baseline

Secondary outcomes

  1. Assess outcomes morbidity and mortality ischemic stroke in correlation with hepatic steatosis .

    Time frame: Baseline

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Bonita R, Beaglehole R. Recovery of motor function after stroke. Stroke. 1988 Dec;19(12):1497-500. doi: 10.1161/01.str.19.12.1497. PubMed 3201508 ↗
  • DeGraba TJ, Hallenbeck JM, Pettigrew KD, Dutka AJ, Kelly BJ. Progression in acute stroke: value of the initial NIH stroke scale score on patient stratification in future trials. Stroke. 1999 Jun;30(6):1208-12. doi: 10.1161/01.str.30.6.1208. PubMed 10356101 ↗
  • Mughal MM, Khan MK, DeMarco JK, Majid A, Shamoun F, Abela GS. Symptomatic and asymptomatic carotid artery plaque. Expert Rev Cardiovasc Ther. 2011 Oct;9(10):1315-30. doi: 10.1586/erc.11.120. PubMed 21985544 ↗
  • Tahmasebpour HR, Buckley AR, Cooperberg PL, Fix CH. Sonographic examination of the carotid arteries. Radiographics. 2005 Nov-Dec;25(6):1561-75. doi: 10.1148/rg.256045013. PubMed 16284135 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 8, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06628700
Lead sponsor
Assiut University
Responsible party
Mostafa Gamal Atef El-sayed (Resident doctor, Assiut University) — Principal investigator
First posted
Oct 8, 2024
Start date
Oct 10, 2024 (estimated)
Primary completion
Oct 10, 2025 (estimated)
Completion
Nov 10, 2025 (estimated)
Last update
Oct 8, 2024

Study contacts

Mostafa G Gamal
Contact
doctormga610@gmail.com
+20 1147731506
Noureldine A Abdelazeem
Contact
noorelhefny@hotmail.com
01005035180
Mostafa A Gamal
principal investigator · Assiut University
Noureldine A Abdelazeem
study director · Assiut University
Bahaa A Osman
study director · Assiut University

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2024. You cannot join it, but the record below documents what was studied.

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