Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07137143

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Adana City Training and Research Hospital

Adana, Yüreğir, Turkey (Türkiye), 01220

Actively Recruiting

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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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