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The effects of analgesia – sedation and delirium protocol on critically ill patients

The effects of implementation of developed analgesia – sedation and delirium protocol on critically ill patients, outcomes in general intensive care unit , Namazi Hospital , Shiraz , 2011

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201011025083N1
Enrollment
200
Registered
2012-04-11
Start date
2011-04-04
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: agitation. Condition 2: delirium. Condition 3: pain. Restlessness and agitation Other delirium Pain, unspecified

Interventions

Intervention 1: Patients in protocol group assessed for pain by NPS/BPS and and for agitation by RASS every one hour and assessed for delirium by CAM ICU every shift . Then patients treated pharmacolo
Treatment - Other
Treatment - Drugs
Patients in protocol group assessed for pain by NPS/BPS and and for agitation by RASS every one hour and assessed for delirium by CAM ICU every shift . Then patients treated pharmacologically and nonp
Patients in control group treated for pain, agitation and delirium as routine

Sponsors

Vice-Chancellor for Research, Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : informed written consent; Age more than 18 years old Exclusion criteria :length of stay in ICU less than 48 hours; patients who expected to expire in less than 48 hours; use of paralyzing agents, psychiatric problems ; inability to move hands( cast, paralyzed hands, cord injery) , addiction

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
ICU length of stay. Timepoint: total duration of stay in ICU. Method of measurement: check list.

Secondary

MeasureTime frame
Duration of mechanical ventilation. Timepoint: every one hour. Method of measurement: check list.;Delirium. Timepoint: every shift( morning - evening - night. Method of measurement: CAM ICU check list.;Total amount of medication used to treat pain. Timepoint: every one hour. Method of measurement: check list.;Total amount of medication used to treat agitaton. Timepoint: every one hour. Method of measurement: check list.;Total amount of medication used to treat delirium. Timepoint: every one hour. Method of measurement: check list.;Agitation. Timepoint: every one hour. Method of measurement: Richmind Agitation Sedation Scale (RASS).;Ventilator- free days at day 28. Timepoint: every one hour. Method of measurement: check list.;Mortality rate. Timepoint: at the end of study. Method of measurement: check list.;Self extubation. Timepoint: every one hour. Method of measurement: check list.;Pain. Timepoint: every one hour. Method of measurement: Numeric Pain Scale(NPS)- Behavioral Pain Scale (BPS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Mansoori

Shiraz University of Medical Sciences

mansoorip@sums.ac.ir+98 71 1647 4254

Outcome results

None listed

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