- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05151237
Incidence of Perioperative Hypothermia in Adults
December 8, 2021 updated by: Ruslan Abdullayev, Marmara University
Incidence of Perioperative Hypothermia and Associated Risk Factors in Adults
Perioperative hypothermia is associated with many complications, including surgical site infections, delayed wound healing, coagulopathy, prolonged hospital and intensive care unit length of stay.
Perioperative close monitoring of the body temperature is important, and this is recommended by many clinical practice guidelines.
In this study the investigators aimed to detect the incidence of perioperative hypothermia in adult patients in the operating room, and to detect the possible associated risk factors.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
290
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pendik
-
Istanbul, Pendik, Turkey, 34899
- Marmara University School of Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The patients scheduled for any elective operation (except for open heart surgery) will be recruited.
Description
Inclusion Criteria:
- Any elective operation
- ASA I-III physical status
Exclusion Criteria:
- Emergency operations
- ASA IV-V physical status
- Open heart surgeries
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Body temperature
Time Frame: Perioperative
|
Body temperature of the patients will be measured via infrared termometer.
|
Perioperative
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 1, 2021
Primary Completion (Actual)
September 1, 2021
Study Completion (Actual)
November 1, 2021
Study Registration Dates
First Submitted
November 25, 2021
First Submitted That Met QC Criteria
November 27, 2021
First Posted (Actual)
December 9, 2021
Study Record Updates
Last Update Posted (Actual)
December 10, 2021
Last Update Submitted That Met QC Criteria
December 8, 2021
Last Verified
December 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 09.2021.296
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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