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Dexmedetomidine Infusion Dose Versus Rapid Bolus Dose Before Tracheal Intubation.

K

Kasr El Aini Hospital

Status and phase

Enrolling
Phase 2

Conditions

Dexmedetomidine
Intubation Complication

Treatments

Drug: Dexmedetomidine bolus
Drug: Propofol
Drug: Atropine Sulfate
Drug: Dexmedetomidine infusion
Drug: Ephedrine

Study type

Interventional

Funder types

Other

Identifiers

NCT06327399
MS-373-2023

Details and patient eligibility

About

Dexmedetomidine bolus dose may provide similar or less hemodynamic changes (less bradycardia and less hypertension) than infusion dose during induction of anaesthesia and tracheal intubation.

Full description

Preoperative assessment of all patients undergoing elective surgical procedures under general anaesthesia comprises history taking, clinical examination, laboratory testing (complete blood count, kidney function tests, liver function tests), electrocardiogram, and chest X-ray. The study protocol will be explained to the patients, and their consent will be obtained. The patients will be continuously monitored in the operating room for heart rate, blood pressure, and oxygen saturation (baseline values). Then a 20-gauge cannula will be inserted.

Patients will be randomly assigned into two groups: Group A will receive Dexmedetomidine infusion dose of 1 mcg/kg diluted to 100 ml normal saline infused over 10 minutes and Group B will receive Dexmedetomidine bolus dose of 0.3 mcg/kg diluted to 10 mL normal saline administered intravenously over 60 seconds. Then Patients will be induced with propofol till loss of verbal contact, followed by atracurium 0.5 mg/kg IV. After 3 minutes, tracheal intubation will be performed with an appropriate size of cuffed tracheal tube and connected to end tidal CO2 monitor. After confirmation of bilateral equal air entry, it is connected to mechanical ventilation using isoflurane 1.2% for maintaining anesthesia and keeping end tidal CO2 between 35-40 mmHg, Ringer's solution at a rate 5ml/kg/hour IV will be infused for fluid maintenance. If heart rate falls below 45 bpm, rescue dose (500 mcg) of atropine will be given. If MAP decreases below 50 mmHg, boluses of 10 mg ephedrine will be given, while escalation of MAP will be treated by boluses of 50 mg propofol.

At the end of surgery, the inhaled gas is off and the patient is reversed with neostigmine 0.05mg/kg and atropine 0.01mg/kg, then extubation is done. The two groups will be observed for changes in hemodynamic parameters i.e. heart rate (HR) and mean arterial blood pressure at preinduction period (baseline), after 1 min from dexmeditomedine taking, after induction, at intubation and 1,3,5 and 10 min after intubation. No intervention will be allowed during these 10 minutes and morphine at a dose 0.1mg/kg will be used as analgesia for surgery after 10 minutes.

Enrollment

70 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • ASA I and II patients.
  • Mallampati grade I and II.

Exclusion criteria

  • Patient refusal.
  • Morbid obesity.
  • Predicted difficult airway/unanticipated difficult intubation or laryngoscopic attempt lasting greater than 15 seconds or two attempts or more.
  • Patients with uncontrolled sepsis.
  • Pregnancy or breast feeding.
  • Patients with renal impairment i.e. SCr ≥ 1.5
  • Any patient on regular intake of beta blockers or calcium channel blockers.
  • CNS disorders.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups

Group A
Active Comparator group
Description:
patients will receive Dexmedetomidine infusion dose of 1 mcg/kg over 10 min.
Treatment:
Drug: Dexmedetomidine infusion
Drug: Propofol
Drug: Atropine Sulfate
Drug: Ephedrine
Group B
Active Comparator group
Description:
patients will receive Dexmedetomidine bolus dose of 0.3 mcg/kg over 60 seconds.
Treatment:
Drug: Propofol
Drug: Atropine Sulfate
Drug: Ephedrine
Drug: Dexmedetomidine bolus

Trial contacts and locations

1

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Central trial contact

Ramy m alkonaiesy, MD; Amany H saleh, MD

Data sourced from clinicaltrials.gov

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