Effectivity and Safety Study of Trans-artificial-urethral Resection of Female Urethral Caruncle

Not Applicable

• Conditions: Urethral Caruncle

• Registration Number: NCT02490228
• Lead Sponsor: Peking University First Hospital

Brief Summary

To explore the minimally invasive and exhaustive treatment of female urethral canruncle by using trans-artificial-urethral resection of the canruncle. The investigators plant to recruit patients using this surgical method and study the effectivity of this method.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2015-06-30
• Status Verified: 2015-07
• Study Start: 2015-07
• Study First Submitted QC: 2015-07-01
• Last Update Submitted: 2015-07-01
• Study First Posted: 2015-07-03
• Last Update Posted: 2015-07-03
• Primary Completion: 2016-07

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

• patient with urethral caruncle

Exclusion Criteria

• recurrence urethral caruncle

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Operative time	Up to 6 months
Length of hospital stay	Up to 6 months
Estimated blood loss	Up to 6 months
pathological type	Up to 6 months
Complication incidence rate	Up to 6 months

Secondary Outcome Measures

Name	Time	Method
recurrence-free survival	Up to 12 months