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The effect of Riker sedation-agitation scale on clinical outcomes

The effect of Riker Sedation-Agitation scale on clinical outcomes in patients undergoing coronary artery bypass graft surgery in Imam Ali Hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201209244736N4
Enrollment
116
Registered
2012-11-28
Start date
2012-11-21
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

clinical outcomes.

Interventions

Intervention 1: In this study in intervention group,the researcher assess the sedation and agitation level of patients with Riker scale. optimal level of Riker scale is 3,4 score. Intervention 2: In
Prevention
In this study in intervention group,the researcher assess the sedation and agitation level of patients with Riker scale. optimal level of Riker scale is 3,4 score
In control group is used from routin method. This method is based on the physiologic and behavioral criteria such as vital signs and first awakening.

Sponsors

Kermanshah university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Having coronary artery bypass graft surgery. 2. Having acceptable clinical and paraclinical criteria such as adequate tissue perfusion. 3. Age between 40-70 years old. 4. Lack of visual and listening problems. 5. Left ventricular ejection fraction more than 30%, 5. lack of cerebrovascular accidents. 6. Number of grafts between 1-4 without endarterectomy. Exclusion critera: 1. If the patient suffering from one of these disease after surgery: MI, CVA, coagulopathy, reoperation, dangerous arrhythmia, renal failure, wound infection, mechanical ventilation more than 24hour, need to reintubation, operation time more than 4 hour.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Opium consumption dose. Timepoint: after extubation. Method of measurement: Recorded data of checklist during the intervention.;Ventilation duration. Timepoint: after extubation. Method of measurement: measurment of ventilation time.

Secondary

MeasureTime frame
Delirium incidence. Timepoint: during stay in ICU. Method of measurement: delirium screening checklist in intansive care units.;Lenght of stay in hospital. Timepoint: after discharge from hospital. Method of measurement: time of entry and exit from hospital.;Lenght of stay in ICU. Timepoint: after discharge from ICU. Method of measurement: Based on the time of entry and exit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza pourmirza Kalhori

school of paramedical science

rpourmirza@yahoo.com+98 83 1827 9899

Outcome results

None listed

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