The Association of Pelvic Organ Prolapse Severity and Urinary Symptoms and Sexual Function

Pelvic Organ Prolapse Clinical Trial

Official title:

The Association of Pelvic Organ Prolapse Severity and Urinary Symptoms and Sexual Function

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01776580
• Other study ID #: 201107060RC
• Status: Recruiting
• Phase: N/A
• First received: January 18, 2013
• Last updated: January 24, 2016
• Start date: July 2011
• Est. completion date: December 2017

Study information

• Verified date: January 2016
• Source: National Taiwan University Hospital
• Contact: Ho-Hsiung Lin, MD, PhD
• Phone: +886-2-23123456
• Email: hhlin[@]ntuh.gov.tw
• Is FDA regulated: No
• Health authority: Taiwan: Ministry of Health and Welfare
• Study type: Observational

Clinical Trial Summary

Women with pelvic organ prolapse often accompany with urinary symptoms or sexual dysfunction, and analyzing the association will be helpful to identify the indication of proper management. Therefore, the aim of this study is to identify the above associations by perineal sonography.

Description:

Women with pelvic organ prolapse often accompany with urinary symptoms or sexual dysfunction, and analyzing the association will be helpful to identify the indication of proper management. Therefore, the aim of this study is to identify the above associations by perineal sonography.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 1000
• Est. completion date: December 2017
• Est. primary completion date: December 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 20 Years to 99 Years

Eligibility

Inclusion Criteria:

• all patients with lower urinary tract symptoms and will undergo urodynamic studies

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Lower Urinary Tract Symptoms
• Pelvic Organ Prolapse
• Prolapse
• Sexual Dysfunction

Locations

Country	Name	City	State
Taiwan	Department of Obstetrics & Gynecology, National Taiwan University Hospital	Taipei

Sponsors (1)

Lead Sponsor	Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To assess the correlation of bladder descent and lower urinary tract symptoms.	To assess the correlation of bladder descent and lower urinary tract symptoms, and identify which symptoms is best correlated with bladder descent during Valsalva maneuver.	1 day	No
Secondary	To identify the correlation of bladder descent with sexual dysfunction.	To identify which parameters of sexual dysfunction is best correlated with the bladder descent.	1 year	No