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Clinical Trials in Egypt / NCT03276273
Recruiting Observational

Bispectral-Electroencephalography (EEG) in First Time Hemodialysis

NCT03276273 · tracked via the Priya Life Science Egypt tracker
Sponsor
Suez Canal University
Phase
Observational
Started
2017-05-01
Last updated
2026-04-28

Condition(s) studied

Renal Failure Acute Chronic

Investigational drug(s) / intervention(s)

recording of Bispectral Index

recording of Bispectral Index: recording of Bispectral Index

Study summary

The severity of minimal dialysis disequilibrium syndrome (DDS) is currently detected and graded clinically using clinical criteria. Bispectral Index (BIS), an electroencephalographic (EEG) derived parameter is widely used in anesthesia and Critical Care setting to detect effects of anesthetic/hypnotic drugs. The aim of our study was to assess the discriminative power of BIS monitoring to accurately detect DDS.

Eligibility

Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * First Time renal Dialysis Exclusion Criteria: * subjects' consumption of sedatives/hypnotics psychotropic drugs, or concomitant neurological disorders affecting mental state such as hepatic encephalopathy, stroke, stupor or dementia and renal transplant patients.

Primary outcome measure(s)

  • Change in the Bispectral Index value — Over a period of one year Time point 1= First Hemodialysis, Time point 2= Second Hemodialysis, Time point 3= Third Hemodialysis.
    Interpatient Change in the value of recorded Bispectral Index between patients undergoing first time hemodialysis (differences between patients) and intrapatient (differences in bispectral Index values between the first 3 hemodialysis sections of each recruited patient)

Trial sites (2)

FacilityCityRegionStatus
Dalian Medical University Dalian China Recruiting
Theodor Bilharz Research Institute Cairo Egypt Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03276273 on ClinicalTrials.gov ↗ ← All trials in Egypt