CClinicalTrials.gg
CompletedNCT06907277Updated Apr 2, 2025

Dexmedetomidine Enhancing the Recovery After Cardiac Surgery

An interventional study of Dexmedetomidine and Fentanyl in Post-cardiac Surgery, sponsored by Benha University. Completed at 1 site in Egypt. Open to participants aged 40 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-04-02.

Sponsored by Benha University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Aug 2024, registered Mar 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
75
Allocation
Randomized
Ages
40 Years to 65 Years
Sex
All
01

Study summary

Enhanced Recovery After Surgery (ERAS) aims to facilitate a quicker and smoother recovery period following surgical procedures. The implementation of these protocols may lead to patients returning to their daily activities sooner, experiencing greater satisfaction with their care, and potentially encountering fewer complications, ultimately contributing to shorter hospital stays. However, a common challenge in the postoperative phase is postoperative delirium(POD). This complication can lead to both immediate and long-term cognitive impairments, negatively impact overall health outcomes, and increase the financial burden on the healthcare system. Interestingly, dexmedetomidine, known as DXM, is a medication that selectively targets certain receptors in the brain and offers sedative properties with minimal impact on breathing. This characteristic is noteworthy because it may help regulate sleep patterns and support the preservation of cognitive function during the recovery period.

02

Conditions studied

  • Post-cardiac Surgery
03

In context

Lead sponsor

Benha University is the lead sponsor of 356 studies on the registry; 68 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients of American Society of Anesthesiologists Classification (ASA) grade II-III;
  • Patients who were planned to have Coronary Artery Bypass Graft (CABG);
  • Patients were free of exclusion criteria.

Exclusion criteria

Exclusion Criteria:

  • Patients with preoperative high risk for getting Post Operative Delirium or sleep disorders,
  • Patients with American Society of Anesthesiologists Classification (ASA) grade>III;
  • Patients with heart failure, left ventricle ejection fraction of \<25%,
  • Patients with uncontrolled diabetes mellitus, coagulopathy, or history of uncompensated renal or hepatic diseases
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
75 participants (actual)

Study arms

  • Active comparator
    Group D

    Drug: Dexmedetomidine · Drug: Lidocain

  • Active comparator
    Group F

    Drug: Fentanyl

Interventions

  • DrugDexmedetomidine

    Dexmedetomidine (DXM) loading dose of 0.6 µg/kg followed by DXM infusion given at a rate of 0.4 ml/kg/h and was provided as 0.15 µg/kg/h for 24-h PO.

  • DrugFentanyl

    A bolus of fentanyl 5 µg/kg followed by an intraoperative (IO) fentanyl infusion of 3-5 µg/kg/h that was continued as PO analgesia for 24 hours in a dose of 0.3 µg/kg/h.

  • DrugLidocain

    Lidocaine (LID) loading dose (1 mg/kg) followed by a continuous infusion till 24 h PO as 1.5 mg/kg/h.

06

What researchers measure

Primary outcomes

  1. Significant Enhancement of Post Operative Recovery Levels After Dexmedetomidine Administration in Cardiac Surgery.

    Post-operative recovery was measured on 3 levels: Confusion, Sleep Quality, and Delirium. The study focused primarily on postoperative delirium through the Delirium Index, a 7-item questionnaire that graded the severity of delirium in patients with or without dementia. These seven items assess disorders of attention, thought, consciousness, orientation, memory, perception, and psychomotor activity. Each item is scored on a 0-3 scale, with zero indicating the absence of disturbance, while 1-3 indicates mild, moderate, and severe disturbance of the assessed function for a total score ranging between 0 and 21, and higher scores indicate higher delirium severity.

    Time frame: 3 months

07

Study locations

1 site
  • Benha University
    Banhā, El Qalyoubia 13511, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 2, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06907277
Lead sponsor
Benha University
Responsible party
Mohammed Abd ElRahman Hammed (Assistant Lecturer of Anesthesia, Pain & ICU, Benha University) — Principal investigator
First posted
Apr 2, 2025
Start date
Aug 30, 2024
Primary completion
Dec 1, 2024
Completion
Jan 31, 2025
Last update
Apr 2, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion