Clinical Trials Directory

Trials / Completed

CompletedNCT01691690

Analgesic Effect of IV Acetaminophen in Tonsillectomies

Analgesic Effect of Single Dose Intravenous Acetaminophen in Pediatric Patients Undergoing Tonsillectomy

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
250 (actual)
Sponsor
Nationwide Children's Hospital · Academic / Other
Sex
All
Age
2 Years – 9 Years
Healthy volunteers
Not accepted

Summary

Acetaminophen (paracetamol) is a first-line antipyretic and analgesic for mild and moderate pain for pediatric patients. Its common use (particularly in oral form) is underscored by its wide therapeutic window, safety profile, over the counter accessibility, lack of adverse systemic effects (as compared with NSAIDS and opioids) when given in appropriate doses. Although the exact anti-nociceptive mechanisms of acetaminophen continue to be elucidated, these mechanisms appear to be multi-factorial and include central inhibition of the cyclo-oxygenase (COX) enzyme leading to decreased production of prostaglandins from arachidonic acid, interference with serotonergic descending pain pathways, indirect activation of cannabinoid 1 (CB1) receptors and inhibition of nitric oxide pathways through N-methyl-D-aspartate (NMDA) or substance P. Of the above mechanisms, the most commonly known is that of central inhibition of COX enzymes by which the decreased production of prostaglandins diminish the release of excitatory transmitters of substance P and glutamate which are both involved in nociceptive transmission (Anderson, 2008; Smith, 2011). To date, several studies have shown acetaminophen's opioid sparing effect in the pediatric population when given by the rectal or intravenous routes (Korpela et al, 1999; Dashti et al, 2009; Hong et al, 2010).

Detailed description

Once enrolled, subjects will have a standardized anesthetic on the day of surgery: 1. Pre-medication with oral midazolam (0.5mg/kg to maximum dose of 20mg) given 15-20 minutes before induction 2. Inhalation induction with sevoflurane and a mixture of N20/02 3. Propofol 1-1.5 mg/kg to facilitate endotracheal intubation 4. Morphine 0.1 mg/kg given prior to intubation 5. Maintenance anesthesia with isoflurane, titrated to 0.8-1 Minimal Anesthetic Concentration (MAC) with a mixture of Air/02 6. Acetaminophen IV (15 mg/kg) vs. saline placebo infused intraoperatively (randomized by pharmacy) 7. Ondansetron (0.15 mg/kg, maximum dose of 4 mg) and dexamethasone (0.25 mg/kg, maximum dose of 20 mg) for postoperative nausea prophylaxis. Following surgery and extubation, baseline vitals will be obtained and pain scores will be assessed in the post anesthesia care unit (PACU) via Faces, Legs, Activity, Cry, Consolability Scale (FLACC).The presence of emergence delirium will be assessed via Pediatric Agitation and Emergence Delirium scale (PAED). Those subjects whose pain score is assessed at \< 4 will receive standard postoperative care and no analgesics. Assessed pain scores \> 4 will receive 0.5mcg/kg fentanyl q10 minutes as needed. Variables such as time to extubation in the PACU, time to first analgesic delivery, pain scores, # times/total dose of opioids given, presence of sedation, nausea/vomiting, duration of oxygen requirement in PACU, whether or not patient was discharged to floor on oxygen and total PACU time will be recorded during the duration of the patient's PACU stay. Subjects will be discharged to the inpatient floor from the PACU once standard discharge criteria have been met. Following discharge from the PACU, standardized analgesics will be given for breakthrough pain (oral oxycodone 0.1mg/kg q4hrs pro re nata (PRN) pain). Enrolled patients will be followed during the duration of their inpatient stay. Duration of oxygen requirement on the floor, pain scores and number of administered oxycodone doses on the floor will be monitored and recorded.

Conditions

Interventions

TypeNameDescription
DRUGAcetaminophen (paracetamol)Acetaminophen IV (15 mg/kg).
DRUGNormal Saline FlushSaline placebo will be infused intraoperatively.
DRUGMidazolamMidazolam (0.5mg/kg to maximum dose of 20mg) given 15-20 minutes before induction.
DRUGSevofluraneSevoflurane for anesthesia induction.
DRUGNitrous Oxide/OxygenCombination of NO2 \& O2 for anesthesia induction.
DRUGPropofolPropofol 1-1.5 mg/kg to facilitate endotracheal intubation.
DRUGMorphineMorphine 0.1 mg/kg given prior to intubation.
DRUGOndansetronOndansetron (0.15 mg/kg, maximum dose of 4 mg) for postoperative nausea prophylaxis.
DRUGDexamethasoneDexamethasone (0.25 mg/kg, maximum dose of 20 mg) for postoperative nausea prophylaxis.

Timeline

Start date
2012-10-01
Primary completion
2015-11-01
Completion
2016-07-01
First posted
2012-09-25
Last updated
2017-04-06
Results posted
2017-04-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01691690. Inclusion in this directory is not an endorsement.