NCT05151237

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
290

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2021

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2021

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2021

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2021

Completed
24 days until next milestone

First Submitted

Initial submission to the registry

November 25, 2021

Completed
14 days until next milestone

First Posted

Study publicly available on registry

December 9, 2021

Completed
Last Updated

December 31, 2024

Status Verified

December 1, 2021

Enrollment Period

1 month

First QC Date

November 25, 2021

Last Update Submit

December 28, 2024

Conditions

Keywords

hypothermiaperioperativeintraoperativepostoperative

Outcome Measures

Primary Outcomes (1)

  • Body temperature

    Body temperature of the patients will be measured via infrared termometer.

    Perioperative

Interventions

The patients' body temperature will be measured pre-, intra- and post-operatively via an infrared thermometer.

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The patients scheduled for any elective operation (except for open heart surgery) will be recruited.

You may qualify if:

  • Any elective operation
  • ASA I-III physical status

You may not qualify if:

  • Emergency operations
  • ASA IV-V physical status
  • Open heart surgeries

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Marmara University School of Medicine

Istanbul, Pendik, 34899, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Hypothermia

Condition Hierarchy (Ancestors)

Body Temperature ChangesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Ruslan Abdullayev

    Marmara University Department of Anesthesiology and Reanimation

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assist. Prof.

Study Record Dates

First Submitted

November 25, 2021

First Posted

December 9, 2021

Study Start

August 1, 2021

Primary Completion

September 1, 2021

Study Completion

November 1, 2021

Last Updated

December 31, 2024

Record last verified: 2021-12

Data Sharing

IPD Sharing
Will not share

Locations