ClinicalTrials.gg
CompletedNCT03250936TRAUMPOUpdated Aug 29, 2017

Descriptive Study of Trampoline Accidents in the Pediatric Emergency Department of Rennes

An observational study in Trauma, Emergencies and Child, Only, sponsored by Rennes University Hospital. Completed at 1 site in France. Open to participants aged 2 Years to 16 Years. Per ClinicalTrials.gov, last updated 2017-08-29.

Sponsored by Rennes University Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
4,000
Ages
2 Years to 16 Years
Sex
All
01

Study summary

The aim of this study is to compare trauma related to others sport to trauma due to trampoline in pediatric emergencies of Rennes.

Read the detailed description

Trampoline accidents are increasing since a few years. In Rennes hospital, pediatric emergencies are experiencing a subjective increase in admissions for trampoline trauma with increasingly early ages and severe trauma. The aim of this study is to compare trauma related to others sport to trauma due to trampoline in pediatric emergencies of Rennes.

In parallel, retrospective data analysis will be performed on the same data during the year 2008, to compare with a period before the explosion of trampoline sales.

02

Conditions studied

  • Trauma
  • Emergencies
  • Child, Only

Keywords

  • trampoline
03

In context

Wounds and Injuries

2,217 studies on the registry are indexed under Wounds and Injuries; 441 are open to participants now.

This study's enrollment of 4,000 is above the median of 169 across 690 observational studies indexed under Wounds and Injuries.

Browse Wounds and Injuries studies →

Lead sponsor

Rennes University Hospital is the lead sponsor of 451 studies on the registry; 51 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
2 Years to 16 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Children between 2 and 16 years old consulting in pediatric emergencies for a trauma related to trampoline Children between 2 and 16 years old consulting in pediatric emergencies for a trauma related to others sport

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Child from 2 to 16 years old
  • Childs admitted in emergencies unit for a trauma
  • Parents not opposed in their child's participation to the study

Exclusion criteria

Exclusion Criteria:

  • Child under 2 years old (before learning to walk)
  • Single wounds and head injuries not related to sports activities (Fall from a bed or from its height, simple wound with sharp objects)
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
4,000 participants (actual)
Patient registry
No

Groups and cohorts

  • Trampoline group

    Child patients with trauma due to trampoline from june 2016 to december 2016 consulting in emergencies unit of Rennes' hospital

  • Control group

    Child patients with trauma related to sport from june 2016 to december 2016 consulting in emergencies unit of Rennes' hospital

06

What researchers measure

Primary outcomes

  1. Types of trauma related to trampoline compared to trauma related to others sport in pediatric emergencies of Rennes.

    Types of trauma related to trampoline compared to trauma related to others sport in pediatric emergencies of Rennes.

    Time frame: 6 months

Secondary outcomes

  1. Arguments for preventive management in the general practitioner

    Arguments for preventive management in the general practitioner

    Time frame: 6 months

07

Study locations

1 site
  • Pediatric and orthopedic surgery division
    Rennes, 35033, France
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Dec 2016 to primary completion in Jan 2017, 1 month.

Of 265 non-industry observational studies under Wounds and Injuries, half reached primary completion within 28 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 60. This study's 1 month is below that.

Counting every sponsor, half of 312 studies reached it within 28 months; a quarter within 12 and three quarters within 60.

Wounds and Injuries covers many different conditions, not one, so the studies compared here vary widely. Read these figures as a rough guide.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 11, 2017
First posted
Aug 16, 2017
StartActual
Dec 6, 2016
Primary completionActual
Jan 31, 2017
CompletionActual
Jan 31, 2017
Last update
Aug 29, 2017
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 29, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03250936
Responsible party
Sponsor
First posted
Aug 16, 2017
Start date
Dec 6, 2016
Primary completion
Jan 31, 2017
Completion
Jan 31, 2017
Last update
Aug 29, 2017

Study contacts

Bernard Fraisse, Dr
principal investigator · Rennes University Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2017. You cannot join it, but the record below documents what was studied.

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