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Comparison of Intraurethral lidocaine gel with and without nitrous oxide and oxygen mixture inhalation on rigid cystoscopy for pain management

Phase 3
Conditions
Inclusion Criteria1.Patient who was performed by use rigid cystoscopy size 22 Fr2.Patient who was performed by use rigid cystoscopy size 22 Fr with tissue biopsy at bladder mucosa3.Patient who was performed by use rigid cystoscopy size 22 Fr with ureteral insertion size 6 Fr4.Femal and male patients age above 18 Yrs old
Pain
Cystoscopy
Entonox
Registration Number
TCTR20211106001
Lead Sponsor
/A
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending (Not yet recruiting)
Sex
All
Target Recruitment
54
Inclusion Criteria

1.Patient who was performed with Rigid Cystoscopy for diagnosis (22 Fr Size)
2.Patient who was performed with Rigid Cystoscopy and bladder biopsy for diagnosis (22 Fr Size)
3.Patient who was performed with Rigid Cystoscopy and ureteral stent insertion (22 Fr for Rigid Cystoscopy and 6 Fr for ureteral stent)

Exclusion Criteria

1.patient who refuse this project
2.History of lidocaine or nitrous mixture halation allergy
3.patient with impairing pain perception
4.patient with maxillofacial injury
5.patient with pneumothorax

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain Control every 15 minutes during cystoscopy and after immediate cystoscopy and 15 minutes after that Numeric rating Scale
Secondary Outcome Measures
NameTimeMethod
Side Effect of Enotonox 1 Year Questionnaire interview
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