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Trials / Recruiting

RecruitingNCT07411794

Dexmedetomidine vs Midazolam in Coronary Artery By-pass Surgery

A Comparative Evaluation of Dexmedetomidine and Midazolam ınfusions With Respect to Postoperative Delirium in Patients Undergoing Coronary Artery Bypass Grafting

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Cumhuriyet University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim is to compare the incidence of postoperative delirium following coronary artery bypass grafting (CABG) between patients receiving dexmedetomidine and those receiving midazolam infusions.

Detailed description

Patients will be allocated into two groups. Those receiving intraoperative dexmedetomidine infusion will constitute Group D (n = 30), while those receiving intraoperative midazolam infusion will constitute Group M (n = 30). Demographic data, including age, sex, and body mass index, will be recorded. Intraoperative heart rate, mean arterial pressure, SpO₂, bispectral index (BIS), and cerebral oxygenation values will be documented at predetermined intervals. Changes in pCO₂ levels will also be recorded. Surgical duration, cardiopulmonary bypass time, recovery time, length of intensive care unit stay, and the presence of delirium as assessed by the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) will be documented.

Conditions

Interventions

TypeNameDescription
DRUGIntravenous Dexmedetomidine infusion + Standard AnesthesiaFollowing the induction of standard general anaesthesia, dexmedetomidine will be administered as a continuous intravenous infusion at a dose of 0.3-0.7 µg/kg/h.
DRUGintravenous midazolam infusion + Standard anesthesiaFollowing the induction of standard general anaesthesia, midazolam will be administered as a continuous intravenous infusion at a dose of 0.03-0.06 mg/kg/h.

Timeline

Start date
2026-01-15
Primary completion
2026-06-01
Completion
2026-06-15
First posted
2026-02-17
Last updated
2026-02-17

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07411794. Inclusion in this directory is not an endorsement.