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The effect of rewarming on hemodynamic parameters and cognitive state in patients after open heart surgery

Study of the effect of rewarming on hemodynamic parameters and cognitive state in patients after open heart surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100124003146N8
Enrollment
80
Registered
2019-10-19
Start date
2019-08-21
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

Hemodynamic parameters of the patient undergoing open heart surgery- cognitive state of the patient undergoing open heart surgery.

Interventions

Intervention 1: Intervention group: Use of a warm mattress at the time of entering the patient to intensive care unit until the body temperature reaches 37 ° C after open heart surgery.in this method

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Having informed consent for participating in study Gaining MMSE score of more than 24 at the beginning of the study Patients candidate for elective Open-Heart surgery Not having Intra-Aortic Balloon Pump before the surgery

Exclusion criteria

Exclusion criteria: Prolongation of intubation (more than 12 hours) for respiratory problems Opened chest for postoperative reasons Having Intra-Aortic Balloon Pump after the surgery post-operative re-intubation Patients who underwent the surgery of aneurysm or dissection of aorta patient death Return to operating room for any reason Prolonged surgery for more than 5 hours Patients undergoing emergency open heart surgery

Design outcomes

Primary

MeasureTime frame
Mean arterial pressure. Timepoint: Before the intervention at the time of entering of the patient to the ICU, every 30 minutes (at the first hour of intervention), every hour (for 4 hours after the intervention). Method of measurement: monitor.;Systolic blood pressure. Timepoint: Before the intervention at the time of entering of the patient to the ICU, every 30 minutes (at the first hour of intervention), every hour (for 4 hours after the intervention). Method of measurement: monitor.;Diastolic blood pressure. Timepoint: Before the intervention at the time of entering of the patient to the ICU, every 30 minutes (at the first hour of intervention), every hour (for 4 hours after the intervention). Method of measurement: monitor.;Central venous pressure. Timepoint: Before the intervention at the time of entering of the patient to the ICU, every 30 minutes (at the first hour of intervention), every hour (for 4 hours after the intervention). Method of measurement: monitor.;Heart rate. Timepoint: Before the intervention at the time of entering of the patient to the ICU, every 30 minutes (at the first hour of intervention), every hour (for 4 hours after the intervention). Method of measurement: monitor.;Temperature. Timepoint: Before the intervention at the time of entering of the patient to the ICU, every 30 minutes (at the first hour of intervention), every hour (for 4 hours after the intervention). Method of measurement: temperature probe of monitor.;Urine output. Timepoint: Before the intervention at the time of entering of the patient to the ICU, every hour (for 4 hours after the intervention). Method of measurement: urinary bag.;Drainage. Timepoint: Before the intervention at the time of entering of the patient to the ICU, every hour (for 4 hours after the intervention). Method of measurement: Drainage bottle.;Cognitive state. Timepoint: Before the intervention and one week after surgery. Method of measurement: MMSE questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEsmail Azizi

Kashan University of Medical Sciences

azizi_es@kaums.ac.ir+98 31 5554 0022

Outcome results

None listed

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