Viewing Study NCT06569004



Ignite Creation Date: 2024-10-26 @ 3:38 PM
Last Modification Date: 2024-10-26 @ 3:38 PM
Study NCT ID: NCT06569004
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-01-15

Brief Title: IR Beam Used Before Peripheral Intravenous Catheter Application on Vein Visibility
Sponsor: None
Organization: None

Study Overview

Official Title: Karadeniz Technical University - Tubitak Student Project
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The study will be conducted in the Oncology and Cardiovascular Surgery CVS services of a university hospital In the research 30 patients will constitute the control group and 30 patients will constitute the experimental group A nurse working in the clinics where the study will be conducted will perform the PIVK procedure and we will randomly select the control and experimental groups and apply light to the area where the PIVK will be applied to the patients in the experimental groups with a flashlight that emits infrared rays for 10 minutes The nurse will not be aware of whether the radiation application was made to the patient or not The veins will be evaluated by the nurse performing PIVK We will fill out the necessary forms in ANNEX 1 control group and APPENDIX 2 experimental group while the PIVK procedure is applied After the procedure is completed the patients pain anxiety and satisfaction level during the procedure will be marked The data will be entered into the SPSS program and evaluated with statistical tests According to the results the effect of IR rays used before PIVK application on the patients pain anxiety and satisfaction and on the procedure time spent by the nurse for the application will be determined
Detailed Description: A nurse from the ward where the study will be conducted will be contacted and a meeting of approximately 20 minutes will be held about the study The nurse will fill out the forms before and after inserting the catheter into the patient Routine procedures such as tourniquet hand opening and closing will be applied to the control group before catheter application In the experimental group catheter application will be made after the IR beam is applied

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None