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

Peking University First Hospital100 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

100

Conditions

Urethral Caruncle

Interventions

TAURFUCPROCEDURE

female patients with urethral caruncle will receive transurethral resection combine with extension tube.

Eligibility

Sex: FEMALE

Medical Language ↔ Plain English

Inclusion Criteria: \- patient with urethral caruncle Exclusion Criteria: \- recurrence urethral caruncle

Outcomes

Primary Outcomes

Operative time

Time frame: Up to 6 months

Length of hospital stay

Time frame: Up to 6 months

Estimated blood loss

Time frame: Up to 6 months

pathological type

Time frame: Up to 6 months

Complication incidence rate

Time frame: Up to 6 months

Secondary Outcomes

recurrence-free survival

Time frame: Up to 12 months

Central Contacts

Xuesong Li, MD

CONTACT

+86-10-83575101 pineneedle@sina.com

Data from ClinicalTrials.gov

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