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OpenTrials
Completed

NCT Number: NCT03641911

Incidence of Inadequate Pain Treatment in Ventilated Critically Ill Surgical Patients

In SICU, Siriraj hospital there were no protocols place for the management of pain. All decisions were made according the attending physicians.

There were no information about incidence of inappropriate pain management in SICU due to lack of validated tool for assessment.

To date, Thai-version of BPS and CPOT were validated, the incidence of inappropriate pain management in SICU, Siriraj hospital should be assessed.

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Key information

Conditions

Adult ICU Patients Acute Pain Neurologic Manifestations Pain Pain, Acute Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Karuna Wongtangman

Bangkok Noi, Bangkok, 10170, Thailand

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Older than 18 years.
  • Expected duration of mechanical ventilation of more than 24 hours.

Exclusion criteria

  • Quadriplegia.
  • Receiving neuromuscular blocking medications.
  • Coma or severe brain injury
  • Neurosurgery/ CVT patients/ trauma patients

Treatment and study plan

Primary outcomes

  1. overtreatment of pain (Richmond agitation sedation scale)

    Time frame: day0- 2 after admitted to ICU

    Richmond agitation sedation scale -3 to -5 undertreatment NRS 4-10 or CPOT 3-8

  2. inadequate treatment of pain (Numeral rating scale)

    Time frame: day 0-2 after admitted to ICU

    Numeral rating scale 4-10 in communicable patient or critical care pain observation tool 3-8 in non-communicable patients

Secondary outcomes

  1. Mortality rate

    Time frame: 30 days after admitted to ICU

  2. ICU length of stay

    Time frame: 30 days after admitted to ICU

  3. Duration of mechanical ventilation

    Time frame: 30 days after admitted to ICU

  4. Incidence of acquired complication

    Time frame: 30 days after admitted to ICU

    • Ventilator associated pneumonia
    • GI hemorrhage
    • Venous thromboembolism
    • Central venous catheter colonization

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Aug 22, 2018
Registry last updated
Jul 16, 2019

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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