Actively Recruiting
The Effect of Heating the Intensive Care Room in the Early Postoperative Period on Patient Outcomes
Led by Cukurova University · Updated on 2025-08-27
70
Participants Needed
1
Research Sites
27 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study was to evaluate the effect of heating the intensive care room in the early postoperative period on patient outcomes.
CONDITIONS
Official Title
The Effect of Heating the Intensive Care Room in the Early Postoperative Period on Patient Outcomes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who underwent elective abdominal surgery and were admitted to intensive care after surgery
- Patients aged 18 and over
- Patients with body temperature between 36°C and 37.5°C on the morning of surgery
- Patients without pacemaker, dementia, advanced spasticity, muscle atrophy, peripheral lesions, osteoporosis, skin irritation, diabetes, hypertension, or obesity
- Patients not requiring mechanical ventilation
- Patients without illnesses impairing thermoregulation such as head trauma or hypothalamic damage
- Patients not taking medications affecting thermoregulation, such as vasodilators
- Patients without peripheral circulation problems
- Patients who are not alcohol or substance abusers
- Patients without mental retardation
- Patients conscious and oriented to person, time, and place
- Patients who can speak Turkish
- Patients without auditory or visual impairments
- Patients who volunteered for the study
You will not qualify if you...
- Patients who do not meet the sampling criteria
- Patients who develop postoperative complications such as bleeding, intubation, stenosis, necrosis, ileus, dermatitis, or parastomal herniation
- Patients whose relatives do not consent to the study
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Adana City Training and Research Hospital
Adana, Yüreğir, Turkey (Türkiye), 01220
Actively Recruiting
Research Team
C
Cansel Bozer Uludağ, expert
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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