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The effect of implementing the daily awakening protocol

The effect of implementing the daily awakening protocol on the clinical Outcomes of mechanically ventilated patients hospitalized in the intensive care Unit.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240912063017N1
Enrollment
90
Registered
2024-10-28
Start date
2024-09-18
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Intubated patients with reduced consciousness.

Interventions

Intervention 1: Intervention group: The working method in this research will be that in the intervention group, the researcher and if necessary the help of a researcher who has received the necessary
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Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patients must be under mechanical ventilation • The patient must be hospitalized in the ICU for at least one week • Receive sedative drugs in the form of infusion • Age range between 20-60 years • Informed consent from the legal guardian for the patient's participation in the study • GCS score between -6 12. • Apache score between 30-50 • Having a spontaneous breathing effort in addition to mandatory ventilator breaths (the patient is on assisted-controlled or spontaneous modes)

Exclusion criteria

Exclusion criteria: • Receiving neuromuscular blocking drugs during the study.• Sending the patient to the ICU departments of other centers • Hemodynamic instability of the patient with the discontinuation of Sedative drugs Creating conditions where the attending physician prohibits the Discontinuation of sedative drugs during the implementation of The intervention Entering the patient into vegetative life during the implementation Of the intervention

Design outcomes

Primary

MeasureTime frame
Consciousness level of patients using glyco coma scale. Timepoint: Immediately before and after each intervention during the first 7 days of The intervention. Method of measurement: Using the GCS scale immediately before and after each intervention During the first 7 days of the intervention.;Pain intensity of patients. Timepoint: During the first 7 days of the intervention immediately before and after the Intervention using the PBS tool. Method of measurement: During the first 7 days of the intervention immediately before and after the Intervention using the PBS tool.

Secondary

MeasureTime frame
Duration of hospitalization in the intensive care unit. Timepoint: During hospitalization. Method of measurement: During hospitalization.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Adineh

Ahvaz University of Medical Sciences

mohadineh@gmail.com+98 916 159 0775

Outcome results

None listed

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