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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 .

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 .

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201222049801N1
Enrollment
70
Registered
2021-04-14
Start date
2021-05-10
Completion date
Unknown
Last updated
2021-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pain. Pain, not elsewhere classified

Interventions

Intervention 1: Intervention group: At first, nurses measure the restlessness of patients based on the Richmond Instrument (RASS) to assess baseline status. Then, they measure the patient's pain befor

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

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

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)

Design outcomes

Primary

MeasureTime frame
Level 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.—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Kouhi

Mashhad University of Medical Sciences

koohif1@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026