Dexmedetomidine Versus Midazolam-Fentanyl for Analgesia and Sedation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-50
SponsorEgymedicalpedia

About this trial

Postoperative sedation is an essential component in recovery of the patient undergoing cardiac surgery. It facilitates the patient's unawareness of the environment as well as reduce the discomfort and anxiety caused by surgery, intubation, mechanical ventilation, suction, and physiotherapy.

Despite the advances in anesthesia and surgical techniques, the duration of mechanical ventilation (MV) may be prolonged after cardiac surgery, due to the classic high-dose narcotic-based cardiac anesthesia.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

Patient refusal.

Emergent valve cardiac surgeries.

Patients with known hypersensitivity to study drugs.

History of uncontrolled diabetes or hypertension.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Dexmedetomidine

    Drug

    to investigate the postoperative analgesic-sedative effect of dexmedetomidine versus fentanyl-midazolam to achieve fast-track extubation after adult valvular cardiac surgeries.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Dexmedetomidine GroupExperimental treatment 1 intervention
Group B: Fentanyl GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Pain Relieve

Assessment of the pain post-operatively in patients with pain score by VAS as : Total scores vary from 0 to 10 in this method, with a higher score indicating more severe pain

Time frame
2 hours post operative

Secondary outcomes

Other outcomes

Sponsors and contacts

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