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 TolerancePainOpioid Tolerance
- Interventions
- Drug: Placebo
- Registration Number
- NCT01553435
- 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
Group Intervention Description Dextromethorphan, opioid analgisia, efficacy Dextromethorphan - Placebo,opioid analgesia, efficacy Placebo -
- Primary Outcome Measures
Name Time Method Effect of N-methyl D-aspartate (NMDA) receptor antagonist Dextromethorphan on Opiods analgesia and tolerance in Pediatric Intensive Care Unit Patients Two years Control of pain
- Secondary Outcome Measures
Name Time Method Effect of N-methyl D-aspartate (NMDA) receptor antagonist Dextromethorphan on Opiods analgesia and tolerance in Pediatric Intensive Care Unit Patients Two years Length of Hospital Stay in two groups
Trial Locations
- Locations (1)
King Abdul Aziz Medical City
πΈπ¦Riyadh, Central, Saudi Arabia