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Effect of N-methyl D-aspartate (NMDA) Receptor Antagonist Dextromethorphan on Opiods Analgesia and Tolerance in Pediatric Intensive Care Unit Patients

Not Applicable
Conditions
Analgesia Tolerance
Pain
Opioid Tolerance
Interventions
Registration Number
NCT01553435
Lead Sponsor
King Abdullah International Medical Research Center
Brief Summary

Effect of N-methyl D-aspartate (NMDA) receptor antagonist Dextromethorphan on Opiods analgesia and tolerance in Pediatric Intensive Care Unit Patients

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
36
Inclusion Criteria

Not provided

Exclusion Criteria
  • Patients under 2 years of age
  • Patients with anticipated PICU length of stay less than 3 days.
  • Patients shall be excluded if Morphine or Fentanyl infusions not continued for the minimum duration of 72 hours after enrollment
  • Patients develops hemodynamic instability
  • Patients with Hepatic failure
  • Withdrawal request by parent(s)/guardian/family

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Dextromethorphan, opioid analgisia, efficacyDextromethorphan-
Placebo,opioid analgesia, efficacyPlacebo-
Primary Outcome Measures
NameTimeMethod
Effect of N-methyl D-aspartate (NMDA) receptor antagonist Dextromethorphan on Opiods analgesia and tolerance in Pediatric Intensive Care Unit PatientsTwo years

Control of pain

Secondary Outcome Measures
NameTimeMethod
Effect of N-methyl D-aspartate (NMDA) receptor antagonist Dextromethorphan on Opiods analgesia and tolerance in Pediatric Intensive Care Unit PatientsTwo years

Length of Hospital Stay in two groups

Trial Locations

Locations (1)

King Abdul Aziz Medical City

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Riyadh, Central, Saudi Arabia

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