Propofol-Dexmedetomine Adjunction in Balanced Anesthesia for Minimally Invasive Cardiac Valve Surgery :Effect on Anesthetic Consumption ,Perioperative Outcomes,and Early Recovery

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age25-60
SponsorKafrelsheikh University

About this trial

Propofol-Dexmedetomidine Adjunction in Balanced Anesthesia for Minimally Invasive Cardiac Valve Surgery: Effects on Anesthetic Consumption, perioperative outcomes, and Early Recovery

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients belonging to American Society of Anesthesiologists (ASA) class I or II

patients scheduled for minimally invasive cardiac valve surgery.

Disqualifiers

patient more than 60 years

patients having neurological/psychological disorders,

patient having severe systemic disorders (renal/hepatic dysfunction and severe respiratory disorder),

patient with history of allergy to the study drugs,

Trial design

Design model

Parallel

Treatments tested in this trial

  • Propofol (Astra-Zeneca)

    Drug

    Thirty patients will receive a continuous infusion of propofol at a rate of 2 mg/kg/h and 50 cc 0.9% sodium chloride solution infused at a rate of 0.4 µg/kg/h (used as a placebo).

  • propofol and dexmetomidine

    Drug

    patients will receive a continuous infusion of propofol at a rate of 2 mg/kg/h in addition to dexmedetomidine at a rate of 0.4 µg/kg/h.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Propofol group (Group P) (control group)Active comparator 1 intervention
Group B: Propofol dexmedetomidine group (Group PD)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

total intraoperative isoflurane consumption between propofol dexmedetomidine anesthesia and propofol anesthesia alone under entropy-guided anesthesia

Total intraoperative isoflurane consumption Description: The total amount of isoflurane consumed during anesthesia will be compared between patients receiving propofol-dexmedetomidine anesthesia and those receiving propofol anesthesia alone under entropy-guided anesthesia. Isoflurane consumption will be assessed from induction of anesthesia until discontinuation of anesthesia and measured as the total volume consumed. (ML\\MIN)

Time frame
Time Frame: From induction of anesthesia until discontinuation of anesthesia; total isoflurane consumption will be recorded at the end of surgery.

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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