Effect of early warning scale for patient transfer outcomes

The effect of the early warning scale versus the conventional method on patient transfer outcomes following open heart surgery.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20221231056998N3

Enrollment

Registered

2025-09-05

Start date

2025-10-23

Completion date

Unknown

Last updated

2025-09-15

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

Conditions

Mechanical complication of heart valve prosthesis. Mechanical complication of heart valve prosthesis

Interventions

Intervention 1: Intervention group: Patients who are transferred from the intensive care unit to the ward using the NEW protocol. Using the early warning scale to assess the patients condition, planni

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients over 18 years of age Candidate for open heart surgery Providing written consent from the patient or their family to participate in the study Patients for whom it is possible to follow the consequences of the transfusion for a certain period Patients with stable condition after surgery Patients with stable cardiovascular status before surgery

Exclusion criteria

Exclusion criteria: Patients with a history of cancer Patients with a history of diabetes Patients with a history of stroke

Design outcomes

Primary

Measure	Time frame
Occurrence of arrhythmia. Timepoint: At the beginning of the study (before the intervention) and immediately after the intervention. Method of measurement: Cardiac monitoring device.;Blood pressure changes. Timepoint: At the beginning of the study (before the intervention) and immediately after the intervention. Method of measurement: Cardiac monitoring device.;Changes in level of consciousness. Timepoint: At the beginning of the study (before the intervention) and immediately after the intervention. Method of measurement: Glasgow Coma Scale.;Return of patients to the ICU. Timepoint: At the beginning of the study (before the intervention) and immediately after the intervention. Method of measurement: Researcher-made questionnaire.;SPO2 changes. Timepoint: At the beginning of the study (before the intervention) and immediately after the intervention. Method of measurement: Cardiac monitoring device.	—

Measure

Time frame

Occurrence of arrhythmia. Timepoint: At the beginning of the study (before the intervention) and immediately after the intervention. Method of measurement: Cardiac monitoring device.;Blood pressure changes. Timepoint: At the beginning of the study (before the intervention) and immediately after the intervention. Method of measurement: Cardiac monitoring device.;Changes in level of consciousness. Timepoint: At the beginning of the study (before the intervention) and immediately after the intervention. Method of measurement: Glasgow Coma Scale.;Return of patients to the ICU. Timepoint: At the beginning of the study (before the intervention) and immediately after the intervention. Method of measurement: Researcher-made questionnaire.;SPO2 changes. Timepoint: At the beginning of the study (before the intervention) and immediately after the intervention. Method of measurement: Cardiac monitoring device.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMalihe sadat Moayed

Bagheiat-allah University of Medical Sciences

msmoayed@gmail.com0218126121

Outcome results

None listed

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