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The Effects of Dexmedetomidine on Postoperative Cognitive Function in Open Heart Surgery

S

Sohag University

Status

Enrolling

Conditions

Neuronal Damage
Open Heart Sugery

Treatments

Drug: Dexmedetomidine

Study type

Interventional

Funder types

Other

Identifiers

NCT06655025
Soh-Med-15-10-1MD

Details and patient eligibility

About

To assess the impact of Dexmedetomidine on postoperative cognitive function and serum Neuron Specific Enolase levels as an indicator of neuronal injury in patients undergoing open heart surgery

Enrollment

32 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

32 participants in 2 patient groups, including a placebo group

Group B (Dexmedetomidine)
Active Comparator group
Description:
Dexmedetomidine infusion
Treatment:
Drug: Dexmedetomidine
Group A (control)
Placebo Comparator group
Description:
normal saline infusion
Treatment:
Drug: Dexmedetomidine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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