Comparing TIVA Using Propofol or Dexmedetomidine Versus Sevoflurane During Anaesthesia of Children Undergoing Bone-Marrow Aspiration
NCT ID: NCT05636566
Last Updated: 2022-12-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2/PHASE3
60 participants
INTERVENTIONAL
2022-02-15
2022-10-25
Brief Summary
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Bone marrow aspiration (BMA) is a frequent procedure that necessitate a meticulous anaesthetic plane that entails rapid non-traumatic induction together with adequate pain free maintenance and instant smooth recovery after a short time practice. Total intravenous anaesthesia (TIVA) had emerged as alternative anaesthetic technique to inhalational anaesthesia for conscious sedation in BMA cited by many authors.
Propofol a popular anaesthetic/ sedative with a rapid onset, short duration and smooth recovery of consciousness and psychomotor functions with no cumulation. However it is poorly analgesic, depresses respiration and there is a possibility of loss of muscle tone leading to airway obstruction .
Dexmedetomidine is a greatly active α2 adrenergic agonist with a valuable anaesthetic- analgesic saving effects. It augments sedation, hypnosis and preservation of muscle tone with negligible respiratory depression and hemodynamic derangements.
The purpose of the current study is to compare between effects of TIVA using propofol or dexmedetomedine versus sevoflurane for maintenance of anaesthesia in children undergoing bone marrow aspiration.
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Detailed Description
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Patients and methods: 60 child aged 3-12 years with ASA physical status I and II planned for elective bone marrow biopsy and aspiration were enrolled randomly into 3 groups 20 child each; group(S): received sevoflurane- oxygen for induction and sevoflurane with fentanyl infusion for maintenance of anaesthesia. Group (P): received propofol for induction followed by propofol-fentanyl infusions for maintenance of anaesthesia. Group (D): received dexmedetomedine infusion for induction followed by dexmedetomedine-fentanyl infusions for maintenance of anaesthesia. The primary endpoint was postoperative sedation score on arrival to the post anaesthetic care unit (PACU) after surgery. Secondary outcomes included procedure duration, hemodynamic variables, parents and surgeons satisfaction and incidences of any adverse events.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
* Group (S): received sevoflurane- oxygen for induction and sevoflurane with fentanyl (Fentanyl, Janssen-Cilag, Germany) infusion for maintenance of anaesthesia.
* Group (P): received propofol (Diprivan, Astra Zeneca, Wedel, Germany) for induction followed by propofol-fentanyl infusions for maintenance of anaesthesia.
* Group (D): received dexmedetomedine (Precedex, Dexmedetomedine HCL inj.,Hospira, Inc.,Lacke Forest, USA) infusion for induction followed by dexmedetomedine-fentanyl infusions for maintenance of anaesthesia. All solutions were prepared by a team member not participating in data recording of the study.
PREVENTION
SINGLE
Study Groups
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Group (S)
sevoflurane inhalational anaesthesia for induction, then sevoflurane and fentanyl infusion for maintenance ,
Sevoflurane
inhalational anaesthesia for maintenance
Group P
propofol infusion for induction afterward propofol and fentanyl infusions for maintenance of anaesthesia
Propofol infusion for maintance
propofol infusion after induction for maintenance of anaesthesia
Group D
dexmedetomedine infusion for induction after that dexmedetomedine and fentanyl infusions for maintenance
Dexmedetomidine
0.5 mic /kg dexmedetomedine is injected after induction of anaesthesia
Interventions
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Sevoflurane
inhalational anaesthesia for maintenance
Propofol infusion for maintance
propofol infusion after induction for maintenance of anaesthesia
Dexmedetomidine
0.5 mic /kg dexmedetomedine is injected after induction of anaesthesia
Eligibility Criteria
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Inclusion Criteria
* both sexes
* ASA physical status I and II
Exclusion Criteria
* with recognized lipid or carbohydrate deranged metabolism
* cardiac dysrhythmias
* congenital heart diseases
* cardiomyopathy
* significant organ dysfunction.
3 Years
12 Years
ALL
No
Sponsors
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Alexandria University
OTHER
Responsible Party
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Locations
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Alexandria University Faculty of Medicin
Alexandria, , Egypt
Countries
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Other Identifiers
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0305414
Identifier Type: -
Identifier Source: org_study_id
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