Could a simple anesthetic shot reduce catheter use after incontinence surgery?
NCT ID NCT03913845
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether using lidocaine (a numbing drug) instead of saline during sling surgery helps women avoid urinary retention. About 150 women with stress incontinence took part. The goal was to see if fewer women need a catheter after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lidocaine with epinephrine
- What this could lead to
- If it works, this could point toward a simple way to reduce the need for catheters after sling surgery, lowering infection risk and improving recovery.
- What could go wrong
- This is a small, completed Phase 4 trial with 150 women, so results may not apply to everyone. Lidocaine's effects are short-lived, and any benefit may be modest.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
150 people
The number who actually took part.
- Started
-
Nov 2019
- Finished
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Nov 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 99 years
- Sex
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Female participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18 years or older * English speaking * Competent to give consent Exclusion Criteria: * A known intolerance or allergic reaction to local anesthetics * Planned spinal anesthesia for the procedure * Planned concomitant prolapse repair other than anterior repair * Preoperative voiding dysfunction as evidenced by a postvoid residual (PVR) of 150 mL or greater.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
AHN Bethel Park Health + Wellness Pavilion
Bethel Park, Pennsylvania, 15102, United States
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AHN Jefferson Hospital
Jefferson Hills, Pennsylvania, 15025, United States
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AHN West Penn Hospital
Pittsburgh, Pennsylvania, 15224, United States
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AHN Wexford Health + Wellness Pavilion
Wexford, Pennsylvania, 15090, United States
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