Effects of Dexmedetomidine on cognitive function after heart surgery

The Effects of Dexmedetomidine on Postoperative Cognitive Function and Neuron-Specific Enolase Levels in Open Heart Surgery

Not applicable Interventional Sohag University · NCT06655025

This study tests if the sedative Dexmedetomidine can help improve thinking skills and reduce brain injury in people having heart surgery.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment32 (estimated)
SexAll
SponsorSohag University Academic / other
Locations1 site (Sohag)
Trial IDNCT06655025 on ClinicalTrials.gov

What this trial studies

This study evaluates how Dexmedetomidine, a sedative medication, influences cognitive function and serum Neuron Specific Enolase levels, which indicate neuronal injury, in patients undergoing elective open-heart surgery. The research aims to determine if this medication can mitigate cognitive decline post-surgery. Patients will be monitored for changes in cognitive abilities and neuronal damage markers following their surgical procedures.

Who should consider this trial

Good fit: Ideal candidates are patients of both sexes scheduled for elective open-heart surgery.

Not a fit: Patients with a history of neurological disorders or severe renal or liver dysfunction may not benefit from this study.

Why it matters

Potential benefit: If successful, this study could lead to improved cognitive outcomes for patients after open-heart surgery.

How similar studies have performed: Other studies have shown promising results with similar approaches, indicating potential for success.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients of both sexes undergoing elective open-heart surgery

Exclusion Criteria:

* Patients with a history of neurological disorders, severe renal or liver dysfunction, or contraindications to Dexmedetomidine as in patients with known QT prolongation, a history of other arrhythmias, symptomatic bradycardia, hypokalemia, or hypomagnesemia, and in patients receiving other drugs known to prolong the QT interval.

Patients with cognitive impairment, mental and psychological illness and chronic alcoholics, drug addicts, abuse of psychotropic substances, illiterate education

Where this trial is running

Sohag

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Open Heart SugeryNeuronal Damage
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.