Evaluation of the effect of pain management program based on critical care pain observation tool (CPOT) on pain intensity and dose adjustment of analgesic in patients with decreased level of consciousness admitted to the intensive care units of Imam Reza Hospital in Mashhad .
Not Applicable
- Conditions
- pain.Pain, not elsewhere classified
- Registration Number
- IRCT20201222049801N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Age 18 to 65 years
Pulmonary patients subgroup (COPD, pneumonia, asthma, etc.)
Inability to communicate verbally
Having a systolic blood pressure greater than 100 mm Hg and a MAP> 65
Earn a score less than or equal to -1 and equal to or greater than -3 on the Richmond scale(-3=RASS=-1)
At least 24 hours intubation and mechanical ventilation
The need to use infusions of sedatives in the treatment program
Admitted in the intensive care unit
Exclusion Criteria
The patient with drug, alcohol and psychotropic abuse
The patients with psychological disorders or history of epilepsy
The patients with neuromuscular disease
The patients with severe structural problems of the brain
Allergy to sedatives (fentanyl, morphine)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evel of Pain. Timepoint: Before procedure and then 5, 15, 30 minutes after the procedures. Method of measurement: using critical care pain observation tool (CPOT) and (Behavioral Pain Scale) BPS.
- Secondary Outcome Measures
Name Time Method