Double Blinded Randomized Trial Between Lidocaine And Plain Gel For Urethral Straight Catheterization And The Q-Tip Test
Completed · Phase 4
Conditions studied: Pain
In brief
The purpose of this study is to compare the pain perception between lidocaine and plain aqueous gel during assessment of postvoid residual volume and the Q-tip test.
Key facts
- Study ID
- NCT00883103
- Run by
- Baystate Medical Center
- People needed
- 137
- Starts
- 2007-11-01
- Expected to finish
- 2008-09-01
- Last updated by the study team
- 2011-09-13
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- All women who presented to a single urogynecologist's office for an initial consultation with a complaint of urinary incontinence and/or pelvic organ prolapse
You may not qualify if…
- Being a minor
- Pregnancy
- Allergy to Lidocaine or aqueous lubricant gel
- Any current use of analgesia
- Structural abnormalities of the urethra
- Active genital Herpes or other vulvovaginal infections or inability to cooperate with pain assessment due to mental disorders.
Where it is running
- Baystate Medical Center — Springfield, Massachusetts, United States
Full record on ClinicalTrials.gov
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