New pap smear device aims to reduce pain and boost screening rates
NCT ID NCT06861504
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new device called the Femscope Calm Collect Device for collecting cervical cells during cancer screening. The goal was to see if it could collect cells just as well as a traditional Pap smear but with less pain and discomfort. Thirteen healthy women aged 21-45 took part, each receiving both the new device and a standard Pap smear for comparison.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Femscope Calm Collect Device
- What this could lead to
- If it works, this device could make cervical cancer screening more comfortable and encourage more women to get tested regularly.
- What could go wrong
- This was a very small, early study with only 13 participants, so results may not apply to everyone. The device may not collect cells as well as the standard method.
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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13 people
The number who actually took part.
- Started
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Dec 2024
- Finished
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Aug 2025
- Lead sponsor
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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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21 to 45 years
- 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: \- Healthy female ages 21-45 with female reproductive organs present at the time of study. Exclusion Criteria: * Pregnancy * Menopausal * Age less than 21 years * Age of 46+ years * History of reproductive cancer * Hysterectomy
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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
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University of Michigan Flint
Flint, Michigan, 48502, United States
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Other studies related to the condition(s) this trial covers.
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