Actively Recruiting

Age: 18Years - 92Years
MALE
NCT06585748

Lidocaine Spray Use on Patients Comfort in Undergoing Bladder Catheterization

Led by Ankara City Hospital Bilkent · Updated on 2024-09-05

100

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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 lower.The 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 patients\' sleep at the end and reduced the feeling of restlessness by reducing pain.

CONDITIONS

Official Title

Lidocaine Spray Use on Patients Comfort in Undergoing Bladder Catheterization

Who Can Participate

Age: 18Years - 92Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Male patients over 18 years old
  • No trauma
  • Spontaneous urine output
  • Oriented and cooperative patients
Not Eligible

You will not qualify if you...

  • Patients under 18 years old
  • Female patients
  • Patients with trauma
  • Patients with globe vesicale requiring rapid catheterization
  • Patients with anatomical variations
  • Patients with urethral-bladder outlet problems preventing catheterization
  • Patients who refuse to participate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ankara Etlik City Hospital

Ankara, Ankara, Turkey (Türkiye), 06170

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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