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Completed

NCT Number: NCT00801203

A Study to Evaluate the Effectiveness of the Induced Reflex Cough Test Plus Urodynamics to Identify Stress Urinary Incontinence in Female Subjects With a History of Stress Urinary Incontinence

This study is to evaluate the effectiveness of identifying stress urinary incontinence (SUI) in female subjects using the Induced Reflex Cough Test (IRCT) administered with urodynamic testing by evaluation of sensitivity and specificity.

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Key information

Age range

25 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Clinical Physiology Associates, Inc, Cape Coral, Florida, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women >25 years of age
  • History of SUI (except for healthy controls)
  • Healthy or stable medical problems (no change in 3 months)
  • Willingness and ability to undergo all the study procedures
  • Stable medications are allowed except for prescription and over-the-counter medications with anticholinergic or α-agonistic properties that can affect the bladder or urethra; these must be discontinued at least 2 weeks prior to evaluation
  • Able to understand and sign the informed consent document.

Exclusion criteria

  • Body mass index (BMI) >40
  • History of severe arthritis of the hips, knees, or feet that could limit mobility during the study
  • Prior treatment of any kind (surgical or pharmacologic) for incontinence at least 30 days before the cough testing session including treatment with slings, botox, interstim and all bulking agents
  • Prior pelvic radiation
  • Post-void residual urine >100 mL at screening
  • Pelvic Organ Prolapse Quantification (POP-Q) stage >2
  • Positive urine culture at screening or dip stick for >1+ leukocyte esterase on the day of the procedures
  • Positive pregnancy test
  • Evidence of infection with hepatitis or human immunodeficiency virus (HIV)
  • Dementia
  • Clinically significant changes on the electrocardiogram (ECG) in women >50 years of age or in the clinical laboratory values as determined by the investigator
  • History of urge symptoms, diagnosis of interstitial cystitis, irritable bowel disease (requiring medications)
  • History of neurological deficit or injury that could affect laryngeal cough reflex, for example, central nervous system related conditions such as stroke or multiple sclerosis, head and neck cancer, major laryngeal surgery
  • History of neurological disorders leading to bladder abnormalities including stroke, Parkinsonism, multiple sclerosis, spinal cord surgery or spinal cord injury
  • Active hemorrhoids or history of recent (within 1 year) rectal surgery
  • Previous major pelvic or abdominal surgery (within 6 months)
  • Tobacco smokers and non-smokers who have >15 pack-year history or frequent (>2 times per week) marijuana smoking
  • Active sexually transmitted disease or genital herpes outbreak or symptomatic pelvic inflammatory disease
  • Pessary in place

Treatment and study plan

IRCT

Drug

Up to two administrations of the IRCT during a single cough testing session

Primary outcomes

  1. Sensitivity to identify SUI in women with a history of SUI and specificity to not identify SUI in healthy women without a history of SUI

    Time frame: Study Day 1

Secondary outcomes

  1. Positive predictive value (PPV) and negative predictive value (NPV) of the IRCT administered with urodynamic testing

    Time frame: Study Day 1

  2. Urodynamic parameters after IRCT and VCT in normal healthy women and women with a history of SUI

    Time frame: Study Day 1

Sponsors and collaborators

Lead sponsor

Pneumoflex Systems, LLC

Industry

Collaborators

  • Ockham Development Group

Registry information

Official study title

A Phase II/III Controlled Study to Evaluate the Effectiveness of the Induced Reflex Cough Test Plus Urodynamics to Identify Stress Urinary Incontinence in Female Subjects With a History of Stress Urinary Incontinence

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Dec 3, 2008
Registry last updated
May 9, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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