Clinical Trials Directory

Trials / Completed

CompletedNCT01432977

Drug Interactions Between Paracetamol and Setrons in Pain Management

Paracetamol and Setrons : Drug Interactions in the Management of Pain After Tonsillectomy in Children

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
72 (actual)
Sponsor
University Hospital, Limoges · Academic / Other
Sex
All
Age
2 Years – 7 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to demonstrate that the association paracetamol / ondansetron is not as effective as the association paracetamol / droperidol in the treatment of pain in children following tonsillectomy. The secondary objectives are to compare opioid consumption (morphine / codeine) and the cumulated incidence of nausea and vomiting between the two groups of patients in the first 24 hours after

Detailed description

Tonsillectomy is a common operation performed in children that is associated with marked pain and a high incidence of nausea and vomiting. Therefore, national and international guidelines have recommended the use of a setron as a prevention to nausea and vomiting and also the systematic administration of paracetamol to help in the control of postoperative pain. However, a potential interaction between setrons and paracetamol has been reported in different animal studies and in human volunteers although its existence has never been found in the clinic. Indeed, several hypotheses are proposed to explain the mechanism of action of paracetamol in the treatment of pain. However, a recent one involves the endocannabinoid system and spinal serotonin receptors. Serotonin receptors are also involved in the mechanism of action of antiemetics such as setrons. Indeed, these drugs are serotonin antagonists. Therefore, the investigators hypothesized that the concomitant administration of paracetamol and ondansetron leads to an interaction that will decrease the analgesic effect of paracetamol. Patients aged 2-7 years old and scheduled for a tonsillectomy will be recruited. They will all receive intraoperatively intravenous paracetamol together with either ondansetron or droperidol. Pain scores using the CHEOPS scale will be recorded for 24 hours. Furthermore, patients will receive i.v. morphine during the operation and in the recovery room if necessary and a non-steroidal anti-inflammatory drug for postoperative pain; on the ward, oral codeine will be administered when needed. Pain scores will be recorded regularly for up to 24 hours together with opioid consumption and the incidence of nausea and vomiting in the same period. Any adverse event will also be recorded.

Conditions

Interventions

TypeNameDescription
DRUGparacetamol /droperidol
DRUGparacetamol / ondansetron

Timeline

Start date
2011-09-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2011-09-13
Last updated
2012-10-31

Locations

2 sites across 1 country: France

Source: ClinicalTrials.gov record NCT01432977. Inclusion in this directory is not an endorsement.