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NCT07248202Completed

Ketamine-lidocaine Versus Ketamine-fentanyl for Induction of Anesthesia in Patients With Left Ventricular Systolic Dysfunction Undergoing Elective Coronary Artery Bypass

A Comparison Between the Effect of Ketamine-lidocaine Versus Ketamine-fentanyl for Induction of Anesthesia on Cerebral Perfusion Guided by Near Infra-red Spectroscopy in Patients With Coronary Artery Disease and Left Ventricular Systolic Dysfunction Undergoing Elective Coronary Artery Bypass Graft Surgery: (A Randomized Controlled Study)

Source: ClinicalTrials.gov · Last updated 7 Aug 2026

Brief summary (registry, in English)

This study compares ketamine/fentanyl versus ketamine/lidocaine in term of their impact on cerebral perfusion during CABG. No prior data address these effects, and the goal is to identify the induction regimen that better preserves cerebral oxygenation.

Status (registry)
Completed
Study type
Interventional
Enrollment
48 (actual)
First submitted
18 Nov 2025
Start date
1 Dec 2025
Primary completion date
25 Jun 2026
Lead sponsor
Cairo University
NCT number
NCT07248202

What you commit to

  • Study type: Interventional
  • Participants enrolled: 48
  • From 1 Dec 2025 to the primary completion date, 25 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • emergency surgery,

Other illness

  • associated chronic stroke, TIA , carotid occlusive disease( due to abnormal vasomotor activity), patients with known neurological impairment (cerebral infarction , dementia ), significant carotid artery stenosis ,
  • valvular heart disease,
  • persistent arrhythmias,
  • congestive cardiac failure,
  • and those with known allergy to any of the study's drugs,
  • severe systemic non-cardiac disease and
  • Patients with dementia or visual or auditory impairment

Other

  • on mechanical ventilation,
  • intra-aortic balloon pump,
  • patients with baseline NIRS reading \< 60%

Who the study is looking for

  • patients with coronary artery disease
  • with moderate to severe left ventricular dysfunction (ejection fraction \< 40%),
  • scheduled for elective CABG surgery

Age in the registry: 21 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Kasr Alainy hospital
Coordinator of this site? Confirm its status
CairoEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.