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OpenTrials
Completed

NCT Number: NCT01348295

Pediatric Ventilatory Care in Finland 2010

This observational study includes questionnaires send to doctors in all units treating pediatric patients with mechanical ventilation in Finland. Additionally all units treating pediatric patients with mechanical ventilation are invited to perform a quality control-like follow up for 3 months. Patient identity data is not collected, and no interventions to treatment are made.

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Key information

Age range

Up to 16 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital of Oulu

Oulu, North Ostrobothnia, 90220, Finland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age under 16 years
  • Mechanical ventilation during the follow up period

Treatment and study plan

observation

Other

No interventions are made. The purpose of the study is to find out current practices used in pediatric mechanical ventilation.

Primary outcomes

  1. The duration of mechanical ventilation

    Time frame: 1-2000 hours

    Compare the duration of mechanical ventilation in different units in Finland

Secondary outcomes

  1. Ventilator parameters

    Time frame: 1-2000hours

    Comparison of ventilator parameters used during mechanical ventilation of children in pediatric-, neonatal- and adult intensive care units.

Sponsors and collaborators

Lead sponsor

University of Oulu

Other

Registry information

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
May 5, 2011
Registry last updated
May 5, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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