Brain Concussion, Traumatic Brain Injury
Conditions
Keywords
Mild traumatic brain injury, Brain concussion, Post-concussion syndrome, Emergency department, Ondansetron
Brief summary
Background: Most patients suffering from mild Traumatic Brain Injury (mTBI) present persistent symptoms at one week post injury. A systematic review showed a paucity of studies for short term outcomes following mTBI. Among potential treatments for mTBI, ondansetron has shown promising results based on clinical experience and a single retrospective study. Objectives: The primary objective of this pilot study is to determine the feasibility of a randomized controlled trial evaluating the effect of ondansetron to decrease post concussion symptoms at one week following mTBI in children. More specifically, this pilot study will evaluate the proportion of participants who complete assessment at one week following intervention. Method: This will be a randomized, double blinded, controlled trial performed among children aged between 8 and 17 years old who sustained a mTBI in the previous 24 hours. Participants visiting the emergency department will be randomized to receive one dose of either ondansetron or placebo. The primary outcome of interest is defined as an increase from pre-concussion baseline of at least 3 symptoms from the Post Concussion Symptom Inventory (PCSI) one week following trauma. Secondary outcomes will include time to full recovery, mean PCSI score, and outcomes at one month following head trauma. The primary analysis will compare the proportion of participants with persistence of symptoms at one week in both groups. The full study sample size was calculated to have 90% power to detect a decrease in the proportion of persistence of symptoms from 50% to 30% with an alpha value of 0.05. Approximately 126 patients will therefore be recruited in each arm. The investigators plan to recruit 30 participants (10% of the final population) for the pilot study. Expected results: This pilot study should confirm the feasibility of the randomized controlled trial by showing that 90% of the recruited participants provide data on the primary outcome at one week following intervention. On the long term, the investigator expect that ondansetron will decrease the proportion of patients sustaining persistent symptoms of concussion from 50% to lower than 30%.
Interventions
DRUGOndansetron
The intervention of interest will be the administration of one dose of oral ondansetron in the emergency department. The dosage will be 8 mg.
DRUGPLacebo
placebo
Sponsors
St. Justine's Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
8 Years to 17 Years
Healthy volunteers
No
Inclusion criteria
1. Children aged between 8 and 17 years old. This will be limited to this small spectrum of age to insure better homogeneity in the evaluation of the participants and streamlining of outcome measures. Also, this is the age group for which our measurement tool has been validated. 2. Occurrence of a mTBI as defined by the presence of a head trauma, a Glasgow coma scale of 13 to 15 and at least one of the three following criteria4 : * Any period of loss of consciousness. * Any loss of memory for events immediately before or after the accident. * Any alteration in mental state at the time of the accident (eg, feeling dazed, disoriented). And the absence of the following criteria: * Post-traumatic amnesia greater than 24 hours. * Glasgow Coma Scale \< 13, 30 minutes post accident. 3. The trauma occurred in the preceding 24 hours.
Exclusion criteria
* 1\. Inability to obtain a proper written informed consent (language barrier, absence of a parental authority, developmental delay, intoxication, patient too confuse to consent according to the treating physician). 2\. Known allergic reaction or intolerance to ondansetron. 3. Known rhythm or cardiac problem, or history of sudden death in the proximal family 4. Patients who are taking a medication which could increase the QT interval. 5. Patients who received ondansetron in the previous 24 hours 6. Any abnormality on radiological studies, including any bleeding in the brain or skull fracture. 7\. Multi-system injuries with treatment requiring admission to hospital or procedural sedation in the ED.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Persistence of post concussive symptoms | 1 week post intervention | Persistence of post concussive symptoms will be defined by an increase from pre-concussion baseline of at least 3 symptoms of the Post Concussion Symptom Inventory (PCSI). The PCSI is a self-report tool evaluating the presence of 25 symptoms (on a 3-point likert scale) for children 8-12 and 26 symptoms on a (7-point likert scale) for children 13-17 years. An increase of two points or more from pre-injury in any symptom is considered clinically significant. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of days of sport activity restriction | 1 month following intervention | — |
| Time before full recovery | One month following intervention | According to the parents |
| Healthcare utilization | One month following intervention | Proportion of participants who consulted a health resource. |
| Side effects | one week and month following intervention | Side effects will include, in addition to symptoms related to mTBI,proportion of participants who complained of diarrhea or constipation (binary answer). |
| Mean number of PCSI symptoms | one week and month following intervention | — |
| Mean number of school days missed | one month following intervention | — |
Other
| Measure | Time frame | Description |
|---|---|---|
| Compliance with study medication | One week following intervention | Proportion of patients who tolerated their medication and proportion of patients randomized to the control group who received ondansetron |
| Proportion of participants who complete the assessment at one week following intervention | One week following intervention | the main objective of the pilot study is to evaluate the feasibility of the randomized controlled trial. Accordingly, the primary outcome of the pilot study will be the proportion of participants who complete the assessment at one week following intervention |
| Proportion of eligible children who were not included | At baseline | This is the proportion of eligible children who were not included and reasons for non-inclusion. |
Countries
Canada
Outcome results
None listed