Viewing Study NCT06585748



Ignite Creation Date: 2024-10-26 @ 3:39 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06585748
Status: RECRUITING
Last Update Posted: None
First Post: 2024-08-28

Brief Title: Lidocaine Spray Use on Patients Comfort in Undergoing Bladder Catheterization
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect of Lidocaine Spray Use on Patients Comfort in Undergoing Bladder Catheterization a Prospectiveobservational controlled Study
Status: 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: Bladder catheterization is a procedure frequently performed in emergency departments and may cause symptoms such as pain and discomfort in patients This study hypothesizes that lidocaine spray application will improve patient compliance and comfort from the outset and facilitate smoother medical procedures In our prospective case-controlled study the patients were divided into two groups Group L lidocaine and Group P placebo Pain conditions after bladder catheterization were evaluated at 0 minutes during the procedure and 15 30 and 60 minutes after the procedure Face Legs Arm Cry Consolability Pain Scale FLACC and Wong-Baker pain scales were used All time periods in Group L FLACC score and Wang Baker scores were found to be statistically significantly lowerThe differences between the first measurement and the measurements at 15-30-60 minutes of the FLACC score were found to be significantly higher in group P than in group L As a result we recommend that lidocaine spray be applied before urinary catheter insertion This study showed that lidocaine spray increased patients39 sleep at the end and reduced the feeling of restlessness by reducing pain
Detailed Description: None

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