Can a lidocaine shot ease biopsy pain? new study says maybe.
NCT ID NCT06546254
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a lidocaine injection into the cervix (paracervical block) reduces pain during endometrial biopsy. 96 women were randomly assigned to receive either lidocaine or a gentle tap with a capped needle (control). The main goal was to see if pain scores were lower with lidocaine. Results could help make this common procedure less painful.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lidocaine
- What this could lead to
- If it works, this could offer a simple way to reduce pain during endometrial biopsy, making the procedure more tolerable.
- What could go wrong
- This is a small, completed trial with only 96 participants. The control group received a tapping sensation, not a placebo injection, so results may not be widely applicable.
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
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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96 people
The number who actually took part.
- Started
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Jun 2025
- Finished
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Jan 2026
- 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 years and older
- Sex
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Female participants only
- Healthy volunteers
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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 * Any participant \> or = age 18 years old presenting for an endometrial biopsy * All parities of patients are eligible * English speaking participants only Exclusion Criteria * Use of pain medication that is not an NSAID or acetaminophen (e.g. opioids, benzos) within past 24 hours * Confirmed pregnancy * Any diagnosed chronic pain syndromes (eg. fibromyalgia, vaginismus, interstitial cystitis) * Contraindication to lidocaine * Misoprostol administration within 24 hours * Previous unsuccessful office attempt at endometrial biopsy by the same practitioner (note of clarification: previous unsuccessful biopsy attempt by a different practitioner will still be eligible)
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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OPG
Toronto, Ontario, M5G 1Z5, Canada
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