Recruiting

Saline vs. Saline

Sponsor:

Tripler Army Medical Center

Code:

NCT00355433

Conditions

Urinary Incontinence

Eligibility Criteria

Sex: Female

Age: 18+

Healthy Volunteers: Accepted

Interventions

Urodymanics

Study Details

Brief summary:

The purpose of this study is to compare first urge, strong urge, and maximum capacity, and perception of discomfort during urodynamic testing between room temperature and body temperate saline. Twenty-four non-pregnant females referred to the urogynecology clinic for bladder testing will be enrolled into the study. Each patient will serve as her own control, undergoing the bladder testing with both room temperature and body temperature saline.

Conditions

Urinary Incontinence

Study ID

NCT00355433

Start date

Jul, 2006

Status verified date

Jul, 2006

Completion date

Jul, 2006

Eligibility Criteria

Eligibility Criteria

Sex: Female

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Females referred to gynecology clinic for urodynamics evaluation with an appropriate indication for bladder testing

Exclusion Criteria:

  • Male subjects and pregnant females

Study Design

Enrollment

24 participants

Allocation

Randomized

Intervention Model

Single group

Primary purpose

Diagnostic

Interventions and Outcome Measures

Interventions

Urodymanics

Primary outcome measure

  • first urge [ Time Frame: undefined ]
  • strong urge [ Time Frame: undefined ]
  • maximum urge [ Time Frame: undefined ]

Central Contacts and Locations

Locations

Tripler Army Medical Center

Recruiting

Tamc, Hawaii, United States, 96859

Principal Investigator:

Micah J Hill, D.O.

More Information

Sponsor

Tripler Army Medical Center

Last update posted

Jul 24, 2006

Last verified

Jul, 2006

Keywords

  • urinary incontinence
  • urodynamics
  • temperature

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Tripler Army Medical Center on 2006-07-24.