Hasan Kalyoncu University
Gaziantep, 27000, Turkey (Türkiye)
NCT Number: NCT05581316
Bloodstream infections and catheter-related infections frequently occur in burn patients. It is important to correctly assess and manage these infections. The present study aimed to investigate the effects of catheter types used in major burn patients on bloodstream infections as well as to predict sepsis status and manage its prognosis using a procalcitonin biomarker.
Looking for future studies?
Notify Me18 year–85 year
All sexes
Interventional
Not applicable
Gaziantep, 27000, Turkey (Türkiye)
Aim:
Bloodstream infections and catheter-related infections frequently occur in burn patients. It is important to correctly assess and manage these infections. The present study aimed to investigate the effects of catheter types used in major burn patients on bloodstream infections as well as to predict sepsis status and manage its prognosis using a procalcitonin biomarker.
Materials and Methods:
A total of 34 patients admitted to the intensive care unit of the Burn Center, December 25th State Hospital, Ministry of Health, between 2019 and 2022, were included in the study conducted at the Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Hasan Kalyoncu University.
Study inclusion criteria
Study exclusion criteria
Patients included in the study were divided into two groups based on whether they used PVCs or CVCs. Patients' procalcitonin, thrombocyte, and leukocyte levels were assessed every other day for 4 weeks, beginning on the first day they were admitted to the burn center. The above examinations at the Laboratories of the December 25th State Hospital, Ministry of Health of the Republic of Turkey, were retrieved retrospectively from the hospital database.
.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
This patients who were included in this study were assessed for four weeks from the first day of hospitalization and taken to the treatment program. All patients who use peripheral venous catheters in this group.
Time frame: Each participant will be evaluated for 4 weeks
blood test
Time frame: Each participant will be evaluated for 4 weeks
blood test
Time frame: Each participant will be evaluated for 4 weeks
blood test
Hasan Kalyoncu University
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07183943
Burns, Wounds and Injuries
Cairo, Egypt
View Trial DetailsNCT06116227
Burns, Wounds and Injuries
Cairo, Egypt
View Trial DetailsNCT07313735
Bandages, Behavior
Van, Turkey, Turkey (Türkiye)
View Trial DetailsNCT03692273
Burns, Cicatrix
Boston, Massachusetts, United States
View Trial Details