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Analgo-Sedative Effects Of Oral, Or Nebulized Ketamine In Pre-schoolers Undergoing Elective Surgery.

Z

Zagazig University

Status and phase

Completed
Early Phase 1

Conditions

Postoperative Analgesia
Conscious Sedation

Treatments

Drug: Ketamine

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

the primary objective of this study is to investigate the sedative, and analgesic effects of oral, or nebulized ketamine as premedication drugs, and providing postoperative analgesia for the preschoolers and decrease their need for systemic analgesia.The secondary objective is to compare each sedation technique after oral, or nebulized ketamine for safety ,and procedural outcomes.

Full description

Preoperative communication, premedication interventions, and being accompanied by parents are useful methods in decreasing preoperative separation anxiety , postoperative psychological trauma, and ensuring smooth induction for preschoolers undergoing elective surgery.

Procedural sedation, and analgesia was defined by O'Donnell as a drug induced state of decreasing awareness, pain, and memory that allowing patient continue his ,or her own protective reflexes, and moving purposefully( O' Donnell etal, 2003).

Ketamine is an anesthetic drug having sedative, and analgesic properties with different routes of administration in children (IV, intramuscular, subcutaneous, oral, rectal, sublingual, intranasal, and nebulized) .

Ketamine produces its analgesic properties in acut pain management from reversible antagonizing the N-methyl-D-aspartate (NMDA)receptors , reducing levels of many proinflammatory mediators in the acute phase, and acting on other non-NMDA pathways that playing important roles in pain, and mood regulation, like its effect on µ-opioid receptors, nicotinic, muscarinic cholinergic, ɣ-aminobutyric acid receptors, activation of high -affinity D2 dopamine receptors, and L-type voltage-gated calcium channels.

The oral route is the most popular than other routes ,as it's safe, efficient, acceptable, and familiar for pediatric patients..

Oral ketamine often requires higher, and frequent doses as it's bioavailability is lower (17-24%) compared to IV (100%),Intramuscular (93%), sublingual/transbuccal(30%), intranasal(25-50%),and inhaler (70%) due to extensive first pass metabolism in liver, and intestine.

Ketamine inhalation is safe, rapid absorption, and affordable route of administration.

Enrollment

62 patients

Sex

All

Ages

3 to 6 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Parents acceptance.
  • Age (3-6) years old.
  • American Society of Anesthesiologist physical status (ASA) I / II
  • Elective surgery of approximately half to one hour duration under general anesthesia.
  • Child With Body Mass Index (BMI) (15-18kg/m²)

Exclusion criteria

  • Parents refusal.
  • Altered mental status, and epilepsy.
  • History of allergy to ketamine.
  • Recent respiratory tract infection.
  • Sever dysfunction of the central nervous system.
  • Increased intracranial pressure, and increased intra-ocular pressure.
  • Cardiac dysrhythmia ,and/or congenital heart disease.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

62 participants in 2 patient groups

oral ketamine
Experimental group
Description:
evaluate sedative,and analgesic effects
Treatment:
Drug: Ketamine
nebulized ketamine
Active Comparator group
Description:
evaluate sedative, and analgesic effects
Treatment:
Drug: Ketamine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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