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Melatonin 10mg for Concussion (PLAYGAME Trial)

Phase 2 & 3
Waitlist Available
Led By Karen M Barlow, MB.ChB
Research Sponsored by University of Calgary
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 2 , 4 and 12 weeks
Awards & highlights

PLAYGAME Trial Summary

PURPOSE: The long-term goal of this line of research is to develop rational, biologically based evidence for the treatment of post-concussion syndrome (PCS) in children. The objective of this application is to examine the effect of melatonin on the symptoms of PCS and its neurobiology using integrated neurodiagnostic techniques in children. OVERVIEW: PCS is a constellation of clinical symptoms including physical (i.e. headaches), cognitive (i.e. memory), and behavioral disturbances. PCS is associated with significant morbidity in the child and his/her family), and yet there are no evidence-based medical treatments available. This suggests an urgent need to develop novel treatment options to improve outcomes for children suffering from PCS. Melatonin has several relevant mechanisms of action, and neuroprotective effects. Recent research suggests that the explanations for persistent PCS symptoms may be due to alterations in neurotransmissions and neuronal circuitry, particularly involving the dorsolateral prefrontal cortex (DLPFC). Investigators have two specific aims: To determine if treatment with melatonin improves PCS in children following mild traumatic brain injury. Hypothesis: treatment of mTBI children with PCS with 3mg or 10mg of oral melatonin for 28 days will result in a decrease in PCS symptoms as compared with placebo. Effects will be dose-dependent and may be independent of sleep effects. Methods: A randomized double blind, placebo controlled trial (RCT); Outcome measure is a PCS symptom questionnaire. A subsequent RCT will then be performed using the optimal melatonin dose at a second centre. To understand the neurophysiological mechanisms of paediatric PCS and assess any resultant effects of treatment with melatonin. Methods: A case-controlled study within the RCT, using functional MRI and Transcranial Magnetic Stimulation to investigate the neurophysiological properties of paediatric mTBI before and after treatment; Treatment groups from the RCT will be compared with two control groups: i) normal controls and ii) asymptomatic mTBI children. SIGNIFICANCE: This study has the potential to 1) provide a safe and effective treatment for PCS and 2) will provide valuable information about the neurophysiological properties of the brain associated with PCS following mTBI in children and how these change with symptom resolution.

Eligible Conditions
  • Concussion
  • Children
  • Post-Concussion Syndrome
  • Traumatic Brain Injury

PLAYGAME Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 2 , 4 and 12 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 2 , 4 and 12 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change on the Post Concussion Symptom Inventory (PCSI)-(8 - 18 years)
Secondary outcome measures
Number of Patient's Adverse Events
Other outcome measures
Change on the Behavior Assessment System for Children (BASC)-2 -Parent
Change on the Child Health Questionnaire (CHQ)
Change on the Post Concussion Symptom Inventory (PCSI)- Parent questionnaire

Side effects data

From 2014 Phase 2 trial • 40 Patients • NCT01114373
42%
Fatigue
39%
Early Morning Wakening
36%
Daytime drowsiness
11%
Weakness
11%
Dizziness
11%
Nausea
11%
Blurred vision
100%
80%
60%
40%
20%
0%
Study treatment Arm
Melatonin
Placebo

PLAYGAME Trial Design

3Treatment groups
Experimental Treatment
Placebo Group
Group I: Melatonin 3mgExperimental Treatment1 Intervention
Melatonin 3mg capsule (low dose arm), once, at night, 28 days
Group II: Melatonin 10mgExperimental Treatment1 Intervention
Melatonin 10mg capsule(high dose arm), oral, once at night, given for 28 days
Group III: Sugar PillPlacebo Group1 Intervention
Sugar Pill, one capsule, once at night, 28 days
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Melatonin
2014
Completed Phase 4
~1150

Find a Location

Who is running the clinical trial?

University of CalgaryLead Sponsor
792 Previous Clinical Trials
869,055 Total Patients Enrolled
Children's Hospital of Eastern OntarioOTHER
126 Previous Clinical Trials
55,383 Total Patients Enrolled
Karen M Barlow, MB.ChBPrincipal InvestigatorAlberta Children's Hospital Research Institute, University of Calgary

Frequently Asked Questions

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~9 spots leftby Apr 2025