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Clinical Trials/IRCT20150919024080N17
IRCT20150919024080N17
Recruiting
Phase 3

Effect of analgesia-sedation protocol on pain, agitation and cardiovascular response of trauma patient in the surgical intensive care unit

Khoram-Abad University of Medical Sciences0 sites84 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Khoram-Abad University of Medical Sciences
Enrollment
84
Status
Recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Khoram-Abad University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Trauma patients (abdominal, chest, orthopedics trauma, and etc.)
  • Patients need a ventilator with a minimum duration of 24 hours connected to the ventilator.
  • Patients separated from the ventilator The minimum duration of separation from the ventilator is 24 hours.
  • Willingness to participate in the study.
  • Being able to self\-report pain or express pain behaviors.
  • level of consciousness equal and above 7
  • The minimum length of hospital stay in the ICU should be 48 hours.
  • No pregnancy.
  • No coagulation disorders

Exclusion Criteria

  • Transfer to home and using palliative care unit (end of life).
  • Plant life, quadriplegia and the need for continuous infusion of nerve blockers and inhaled prostacyclins.
  • Deep sedation to quit alcohol.
  • Need for continuous infusion of sedative or analgesic for more than 24 hours.
  • Patients with permanent brain injury admitted to neurosurgery wards.
  • Deep sedation for treatment of active seizures.
  • Patients in the final stage of kidney and liver failure.
  • Cardiac arrest.
  • Neurovascular injury, burns, ear, nose and throat surgeries, maxillofacial surgery, or plastic surgery to place a flap on the head or neck.

Outcomes

Primary Outcomes

Not specified

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