Is 'Safe' snus actually safe? 30,000-Person study aims to find out
NCT ID NCT07573319
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study uses data from over 30,000 Swedish adults to see if using snus (including newer white nicotine pouches) is linked to heart disease, metabolic problems, and poor mental health, independent of smoking. Researchers will compare current, former, and never-users using advanced imaging and blood tests. The goal is to clarify the mixed evidence on snus safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- snus (including white nicotine pouches)
- What this could lead to
- If clear links are found, this could guide public health advice and regulation around snus use, especially for young people and women.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. Results may be influenced by other lifestyle factors not fully accounted for.
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.
- Participants
-
About 30,154 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2013
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- 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.
Who is studied
Random selection
- Ages
-
50 to 64 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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.
Cohort Size: Over 30,000 men and women. Locations: Recruited across six Swedish university hospitals: Gothenburg, Malmö/Lund, Linköping, Stockholm, Umeå, and Uppsala. Inclusion criteria: * Age 50-64 years at the time of inclusion * Selection: Randomly selected from the Swedish national population register.
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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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Göteborg Universitetssjukhus
Gothenburg, Sweden
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Karolinska Institutet Danderyds Sjukhus
Stockholm, Sweden
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Skanes Universitetssjukhus, Lund Universitet
Lund, Sweden
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Umeå Universitetssjukhus
Umeå, Sweden
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Uppsala Universitetssjukhus
Uppsala, Sweden
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