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CompletedNCT00667550Updated Jul 15, 2010

Lower Urinary Tract and Sexual Function in Women Following Surgery for Colorectal Disorders

An observational study in Lower Urinary Tract Symptoms and Colorectal Disorders, sponsored by University of California, Irvine. Completed at 1 site in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2010-07-15.

Sponsored by University of California, Irvine · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
34
Ages
18 Years and older
Sex
Female
01

Study summary

This is a prevalence study evaluating lower urinary tract, prolapse, bowel, and sexual symptoms in women with a colorectal disorder who are planning to undergo surgery.

The purpose of this study is to identify the number of women who complain of lower urinary tract and bowel problems, including frequency, urgency, urinary incontinence, fecal incontinence, pain with intercourse, and other sexual problems prior to undergoing surgical management for a colorectal disorder.

Read the detailed description

Lower urinary tract symptoms, including urinary incontinence, voiding dysfunction, urgency, frequency, fecal incontinence, as well as sexual dysfunction, are directly affected by surgery for colorectal disorders. Increased risk of injury to the urinary tract is a recognized complication of pelvic surgery. These risks are related to the radical nature of pelvic surgery used to treat certain colorectal disorders, including colorectal malignancies and inflammatory bowel disease.

Few studies have looked at the incidence of lower urinary tract symptoms and sexual dysfunction in patients with colorectal conditions before and after surgery.

The primary goal of this study is to determine the prevalence of lower urinary tract symptoms in women undergoing surgery for colorectal ocnditions. We also want to describe the prevalence of these symptoms in different colorectal disorders, and how pelvic surgery impacts these symptoms.

02

Conditions studied

  • Lower Urinary Tract Symptoms
  • Colorectal Disorders

Keywords

  • Lower urinary tract symptoms
  • Colorectal disorders
  • Urinary incontinence
  • Fecal incontinence
  • Voiding dysfunction
  • Urgency frequency
  • Sexual dysfunction
  • Colorectal malignancies
  • Inflammatory bowel disease
03

In context

Lower Urinary Tract Symptoms

406 studies on the registry are indexed under Lower Urinary Tract Symptoms; 110 are open to participants now.

This study's enrollment of 34 is below the median of 179 across 132 observational studies indexed under Lower Urinary Tract Symptoms.

Browse Lower Urinary Tract Symptoms studies →

Lead sponsor

University of California, Irvine is the lead sponsor of 466 studies on the registry; 96 are open to participants now.

Of its 41 completed or terminated interventional studies of FDA-regulated products, 30 (73%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Female patients with a diagnosis of a colorectal disorder requiring surgery. Patients must be able to complete the questionnaires in English as the questionnaires are only available and valid in English.

Inclusion criteria

  • Female subjects with a diagnosis of a colorectal disorder, including rectal prolapse, inflammatory bowel disease such as Crohn's disease, Ulcerative Colitis, and colorectal malignancies planning to undergo surgery
  • Females have English as a primary language

Exclusion criteria

Exclusion Criteria:

  • Subjects less than 18 years of age
  • Subjects unable to give informed consent or complete the validated questionnaires
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
34 participants (actual)
06

Study locations

1 site
  • University of California, Irvine Medical Center
    Orange, California 92868, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 15, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00667550
Lead sponsor
University of California, Irvine
First posted
Apr 28, 2008
Start date
Mar 2008
Primary completion
Mar 2010
Completion
Mar 2010
Last update
Jul 15, 2010

Study contacts

Karen L Noblett, M.D.
principal investigator · University of California, Irvine

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2010. You cannot join it, but the record below documents what was studied.

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