CClinicalTrials.gg
CompletedNCT06927700Updated Mar 4, 2026Results posted

Effects of FDA Authorized Smokeless Tobacco Claims Among US Adults Who Smoke Cigarettes

An interventional study of Modified Risk Claim Type - None and Product Brand - General Snus in Tobacco Product Beliefs and Use, sponsored by Rutgers, The State University of New Jersey. Completed at 1 site in United States. Open to participants aged 21 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-04.

Sponsored by Rutgers, The State University of New Jersey · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
1,257
Allocation
Randomized
Ages
21 Years and older
Sex
All
01

Study summary

This study will be an online survey experiment conducted with adults who smoke cigarettes (ages 21+) to examine their reactions to modified risk advertising claims authorized by the Food \& Drug Administration (FDA) for two smokeless tobacco brands (General Snus and Copenhagen), which describe the lower risks of these products compared to cigarette smoking. The study will compare effects of ads with different two different claim types (i.e. claims about reduced lung cancer risk and claims about reduced risks for multiple disease) versus ads with no reduced-risk claims, and examine effects on message and product perceptions, and interest in using the smokeless tobacco products. This study will also examine how smokers' reactions/interest may vary based on the product brand, and asses prior awareness/exposure to the authorized claims.

02

Conditions studied

  • Tobacco Product Beliefs and Use

Browse trials for

Keywords

  • smokeless tobacco
  • tobacco advertising
  • modified risk claims
  • snus
  • moist snuff
03

In context

Tobacco Use

125 studies on the registry are indexed under Tobacco Use; 64 are open to participants now.

This study's enrollment of 1,257 is above the median of 150 across 119 interventional studies indexed under Tobacco Use.

Browse Tobacco Use studies →

Lead sponsor

Rutgers, The State University of New Jersey is the lead sponsor of 496 studies on the registry; 130 are open to participants now.

Of its 38 completed or terminated interventional studies of FDA-regulated products, 30 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Adults (age 21 and over) who are current established cigarettes smokers (i.e., smoked 100 cigarettes in their lifetime and now smoke every day or somedays), based in the US, members of Ipsos' KnowledgePanel, and have chosen to complete their research panel surveys in English

Exclusion criteria

Exclusion Criteria:

  • Panel participants who do not meet the criteria outlined above will be excluded.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
1,257 participants (actual)

Study arms

  • Other
    Group 1 (General Snus-Control Ads)

    Participants in this group will view 4 ads for the brand General Snus that do not include a modified risk claim.

    Behavioral: Modified Risk Claim Type - None · Behavioral: Product Brand - General Snus

  • Experimental
    Group 2 (General Snus-Multiple Disease Ads)

    Participants in this group will view 4 ads for the brand General Snus that include a modified risk claim about the lower risk of multiple diseases.

    Behavioral: Product Brand - General Snus · Behavioral: Modified Risk Claim Type - Multiple Diseases

  • Experimental
    Group 3 (General Snus- Lung Ads)

    Participants in this group will view 4 ads for the brand General Snus that include a modified risk claim about the lower risk of lung cancer only.

    Behavioral: Product Brand - General Snus · Behavioral: Modified Risk Claim Type - Lung Cancer

  • Experimental
    Group 4 (Copenhagen-Control Ads)

    Participants in this group will view 4 ads for the brand Copenhagen that do not include a modified risk claim.

    Behavioral: Modified Risk Claim Type - None · Behavioral: Product Brand - Copenhagen

  • Experimental
    Group 5 (Copenhagen-Multiple Disease Ads)

    Participants in this group will view 4 ads for the brand Copenhagen that include a modified risk claim about the lower risk of multiple diseases.

    Behavioral: Product Brand - Copenhagen · Behavioral: Modified Risk Claim Type - Multiple Diseases

  • Experimental
    Group 6 (Copenhagen- Lung Ads)

    Participants in this group will view 4 ads for the brand Copenhagen that include a modified risk claim about the lower risk of lung cancer only.

    Behavioral: Product Brand - Copenhagen · Behavioral: Modified Risk Claim Type - Lung Cancer

Interventions

  • BehavioralModified Risk Claim Type - None

    Participants will view smokeless tobacco ads with no modified risk claim (control)

  • BehavioralProduct Brand - General Snus

    Participants will views ads for the smokeless tobacco brand General Snus

  • BehavioralProduct Brand - Copenhagen

    Participants will views ads for the smokeless tobacco brand Copenhagen

  • BehavioralModified Risk Claim Type - Multiple Diseases

    Participants will view smokeless tobacco ads with a claim about lower risks for multiple diseases

  • BehavioralModified Risk Claim Type - Lung Cancer

    Participants will either view smokeless tobacco ads with a modified risk claim about lower risks for lung cancer only

06

What researchers measure

Primary outcomes

  1. General Relative Harm Perception

    Single item measure asking participants how harmful they think daily use of the viewed smokeless tobacco product would be to their health compared to daily cigarette smoking, (1=a lot less harmful, 2=somewhat less harmful, 3=about the same, 4=somewhat more harmful, 5=a lot more harmful). Higher scores mean thinking the viewed smokeless tobacco product is more harmful than cigarettes.

    Time frame: Assessed in survey measures completed immediately after viewing the study stimuli

  2. Perceptions of Perceived Relative Risks of Diseases

    Assessment of perceived risks of getting various smoking related diseases from using the viewed smokeless tobacco product versus from smoking cigarettes. Responses to 6 parallel questions (each asking about a different disease) were averaged together in this composite item. The question stated: "If you used only \[General Snus/Copenhagen - inserted based on brand condition\] or only cigarettes every day, which product would make it more likely that you would get": 1) lung cancer; 2) heart disease; 3) mouth cancer; 4) stroke; 5) chronic bronchitis; 6) emphysema. Response options to each were on a 5 point scale from (1=much more likely with General Snus/Copenhagen to 5=much more likely with cigarettes). Results presented here are based on the averages responses to the six items. Higher scores mean thinking risks are greater from smoking cigarettes than from using the viewed smokeless tobacco product.

    Time frame: Assessed in survey measures completed immediately after viewing the study stimuli

  3. Absolute Harm Perception

    Single item measure asking participants how likely or unlikely they think the viewed smokeless tobacco product would be to cause serious health problems during their lifetime, if they used it every day (from 1=not at all likely to 5=extremely likely). Higher scores mean greater likelihood of thinking the product is harmful to health.

    Time frame: Assessed in survey measures completed immediately after viewing the study stimuli

  4. Product Use Intentions

    Assessment of intentions to use the viewed smokeless tobacco products based on averaging responses to three parallel questions: "Thinking about the ads you saw for \[General Snus or Copenhagen\] products, how interested, in the next 6 months, would you be in: 1) Using or trying these products? 2) Using these products as a way to quit or cut down on your cigarette smoking? 3) Completely switching from cigarettes to these products? Response options to each were on a 5 point scale from (1=not at all interested to 5=extremely interested). Results presented here are based on the averaged responses to these three items. Higher scores mean greater interest in using the products.

    Time frame: Assessed in survey measures completed immediately after viewing the study stimuli

Secondary outcomes

  1. Risk Message Recall

    Participants are asked to recall (yes/no) if the ads they viewed include any statement saying that using the product can lower risks of certain diseases.

    Time frame: Assessed in survey measures completed immediately after viewing the study stimuli

  2. Ad Persuasiveness

    A composite measure based on the average of 6 advertisement perceptions, asking participants to rate whether they agreed or disagreed that they ads they viewed: 1) included important information; 2) were understandable; 3) included believable information; 4) included credible information; 5) included information new to me; 6) make me want to learn more about those products. Response options were on a 6 point agreement scale from 1=strongly disagree to 6=strongly agree. Higher scores mean greater agreement that the ads were effective and persuasive.

    Time frame: Assessed in survey measures completed immediately after viewing the study stimuli

  3. Claim Believability & Credibility

    A composite measure based on the average of 2 claim perception items, asking participants to rate whether they agreed or disagreed that the modified-risk claim in the ads they viewed was : 1) believable 2) credible. Participants responded to this while seeing the claim again on the survey screen. Response options were on a 7 point agreement scale from 1=strongly disagree to 7=strongly agree. Higher scores mean greater agreement that the claims were believable and credible.

    Time frame: Assessed in survey measures completed immediately after viewing the study stimuli

  4. Overall Perceived Claim Persuasiveness

    A composite measure based on the average of 7 claim perception items, asking participants to rate whether they agreed or disagreed that the modified-risk claim in the ads they viewed was : 1) believable; 2) credible; 3) important; 4) new to me; 5) makes me think using this product could be less harmful to my health than smoking; 6) makes me more interested in trying this product; 7) would make me think seriously about completely switching to this product. Participants responded to this while seeing the claim again on the survey screen. Response options were on a 7 point agreement scale from 1=strongly disagree to 7=strongly agree. Higher scores mean greater agreement that participants thought the claim was persuasive/effective.

    Time frame: Assessed in survey measures completed immediately after viewing the study stimuli

  5. Switching Comprehension

    An item assessing participants' understanding of the need to completely switch to the smokeless tobacco product viewed in order to reduce risks. It said: Please answer the next question based on your understanding of the ads you viewed earlier. Based on the ads, \[General Snus OR Copenhagen, inserted based on condition\] can reduce a smoker's health risks if you: (Select all that apply) 1. Use only \[General Snus/Copenhagen\] and not smoke any cigarettes anymore 2. Use \[General Snus/Copenhagen\] and smoke fewer cigarettes than before 3. Use both products (\[General Snus/Copenhagen\] and cigarettes) about equally 4. None of the above 5. I don't know/not sure

    Time frame: Assessed in survey measures completed immediately after viewing the study stimuli

07

Results

Posted Mar 4, 2026

Participant flow

Participant flow — Overall Study
MilestoneGroup 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)
Started213209203209209214
Completed213209203209209214
Not completed000000

Outcome measures

PrimaryGeneral Relative Harm Perception

Single item measure asking participants how harmful they think daily use of the viewed smokeless tobacco product would be to their health compared to daily cigarette smoking, (1=a lot less harmful, 2=somewhat less harmful, 3=about the same, 4=somewhat more harmful, 5=a lot more harmful). Higher scores mean thinking the viewed smokeless tobacco product is more harmful than cigarettes.

Time frame:
Assessed in survey measures completed immediately after viewing the study stimuli
Reported as:
Mean · score on a scale
General Relative Harm Perception
score on a scaleGroup 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)
General Relative Harm Perception3.04 ± 0.792.76 ± 0.812.84 ± 0.833.19 ± 0.883.00 ± 0.822.97 ± 0.78
PrimaryPerceptions of Perceived Relative Risks of Diseases

Assessment of perceived risks of getting various smoking related diseases from using the viewed smokeless tobacco product versus from smoking cigarettes. Responses to 6 parallel questions (each asking about a different disease) were averaged together in this composite item. The question stated: "If you used only \[General Snus/Copenhagen - inserted based on brand condition\] or only cigarettes every day, which product would make it more likely that you would get": 1) lung cancer; 2) heart disease; 3) mouth cancer; 4) stroke; 5) chronic bronchitis; 6) emphysema. Response options to each were on a 5 point scale from (1=much more likely with General Snus/Copenhagen to 5=much more likely with cigarettes). Results presented here are based on the averages responses to the six items. Higher scores mean thinking risks are greater from smoking cigarettes than from using the viewed smokeless tobacco product.

Time frame:
Assessed in survey measures completed immediately after viewing the study stimuli
Reported as:
Mean · score on a scale
Perceptions of Perceived Relative Risks of Diseases
score on a scaleGroup 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)
Perceptions of Perceived Relative Risks of Diseases3.34 ± 0.603.44 ± 0.563.33 ± .713.29 ± .613.29 ± .573.38 ± .53
PrimaryAbsolute Harm Perception

Single item measure asking participants how likely or unlikely they think the viewed smokeless tobacco product would be to cause serious health problems during their lifetime, if they used it every day (from 1=not at all likely to 5=extremely likely). Higher scores mean greater likelihood of thinking the product is harmful to health.

Time frame:
Assessed in survey measures completed immediately after viewing the study stimuli
Reported as:
Mean · score on a scale
Absolute Harm Perception
score on a scaleGroup 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)
Absolute Harm Perception3.49 ± 0.913.10 ± 0.943.43 ± 0.993.60 ± 0.983.35 ± 0.963.58 ± 0.96
PrimaryProduct Use Intentions

Assessment of intentions to use the viewed smokeless tobacco products based on averaging responses to three parallel questions: "Thinking about the ads you saw for \[General Snus or Copenhagen\] products, how interested, in the next 6 months, would you be in: 1) Using or trying these products? 2) Using these products as a way to quit or cut down on your cigarette smoking? 3) Completely switching from cigarettes to these products? Response options to each were on a 5 point scale from (1=not at all interested to 5=extremely interested). Results presented here are based on the averaged responses to these three items. Higher scores mean greater interest in using the products.

Time frame:
Assessed in survey measures completed immediately after viewing the study stimuli
Reported as:
Mean · score on a scale
Product Use Intentions
score on a scaleGroup 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)
Product Use Intentions1.52 ± 0.851.55 ± 0.821.48 ± 0.881.45 ± .831.41 ± .751.36 ± .70
SecondaryRisk Message Recall

Participants are asked to recall (yes/no) if the ads they viewed include any statement saying that using the product can lower risks of certain diseases.

Time frame:
Assessed in survey measures completed immediately after viewing the study stimuli
Reported as:
Count of participants · Participants
Risk Message Recall
ParticipantsGroup 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)
Yes2516314116145157
No18846621936356
SecondaryAd Persuasiveness

A composite measure based on the average of 6 advertisement perceptions, asking participants to rate whether they agreed or disagreed that they ads they viewed: 1) included important information; 2) were understandable; 3) included believable information; 4) included credible information; 5) included information new to me; 6) make me want to learn more about those products. Response options were on a 6 point agreement scale from 1=strongly disagree to 6=strongly agree. Higher scores mean greater agreement that the ads were effective and persuasive.

Time frame:
Assessed in survey measures completed immediately after viewing the study stimuli
Reported as:
Mean · score on a scale
Ad Persuasiveness
score on a scaleGroup 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)
Ad Persuasiveness3.55 ± 0.943.53 ± 0.973.37 ± 1.133.36 ± 1.023.22 ± 0.953.34 ± 1.00
SecondaryClaim Believability & Credibility

A composite measure based on the average of 2 claim perception items, asking participants to rate whether they agreed or disagreed that the modified-risk claim in the ads they viewed was : 1) believable 2) credible. Participants responded to this while seeing the claim again on the survey screen. Response options were on a 7 point agreement scale from 1=strongly disagree to 7=strongly agree. Higher scores mean greater agreement that the claims were believable and credible.

Time frame:
Assessed in survey measures completed immediately after viewing the study stimuli
Reported as:
Mean · score on a scale
Claim Believability & Credibility
score on a scaleGroup 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)
Claim Believability & Credibility—3.56 ± 1.553.88 ± 1.74—2.83 ± 1.553.91 ± 1.68
SecondaryOverall Perceived Claim Persuasiveness

A composite measure based on the average of 7 claim perception items, asking participants to rate whether they agreed or disagreed that the modified-risk claim in the ads they viewed was : 1) believable; 2) credible; 3) important; 4) new to me; 5) makes me think using this product could be less harmful to my health than smoking; 6) makes me more interested in trying this product; 7) would make me think seriously about completely switching to this product. Participants responded to this while seeing the claim again on the survey screen. Response options were on a 7 point agreement scale from 1=strongly disagree to 7=strongly agree. Higher scores mean greater agreement that participants thought the claim was persuasive/effective.

Time frame:
Assessed in survey measures completed immediately after viewing the study stimuli
Reported as:
Mean · score on a scale
Overall Perceived Claim Persuasiveness
score on a scaleGroup 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)
Overall Perceived Claim Persuasiveness—3.51 ± 1.193.47 ± 1.33—2.86 ± 1.263.31 ± 1.29
SecondarySwitching Comprehension

An item assessing participants' understanding of the need to completely switch to the smokeless tobacco product viewed in order to reduce risks. It said: Please answer the next question based on your understanding of the ads you viewed earlier. Based on the ads, \[General Snus OR Copenhagen, inserted based on condition\] can reduce a smoker's health risks if you: (Select all that apply) 1. Use only \[General Snus/Copenhagen\] and not smoke any cigarettes anymore 2. Use \[General Snus/Copenhagen\] and smoke fewer cigarettes than before 3. Use both products (\[General Snus/Copenhagen\] and cigarettes) about equally 4. None of the above 5. I don't know/not sure

Time frame:
Assessed in survey measures completed immediately after viewing the study stimuli
Reported as:
Count of participants · Participants
Switching Comprehension
ParticipantsGroup 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)
Use only [General Snus/Copenhagen] and not smoke any cigarettes anymore3998834110289
Use [General Snus/Copenhagen] and smoke fewer cigarettes than before253216161824
Use both products ([General Snus/Copenhagen] and cigarettes) about equally9312976
None of the above9644651035066
I don't know554735444036

Adverse events

Collected over One month. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Group 1 (General Snus-Control Ads)0/213 (0%)0/213 (0%)0/213 (0%)
Group 2 (General Snus-Multiple Disease Ads)0/209 (0%)0/209 (0%)0/209 (0%)
Group 3 (General Snus- Lung Ads)0/203 (0%)0/203 (0%)0/203 (0%)
Group 4 (Copenhagen-Control Ads)0/209 (0%)0/209 (0%)0/203 (0%)
Group 5 (Copenhagen-Multiple Disease Ads)0/209 (0%)0/209 (0%)0/209 (0%)
Group 6 (Copenhagen- Lung Ads)0/214 (0%)0/214 (0%)0/214 (0%)

Baseline characteristics

Age, Continuous
Age, Continuous(years)Group 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)Total
Mean53.6 (21 to 84)53.5 (26 to 81)54.5 (21 to 82)53.9 (22 to 85)54.1 (24 to 87)54.5 (24 to 90)54 (21 to 90)
Sex/Gender, Customized
Sex/Gender, Customized(Participants)Group 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)Total
Male1061059998109102619
Female107104104111100112638
Race/Ethnicity, Customized
Race/Ethnicity, Customized(Participants)Group 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)Total
White, Non-Hispanic171157143135156156918
Black, Non-Hispanic252529412526171
Other, Non-Hispanic286641238
Hispanic122921261919126
2+ Races, Non-Hispanic33415117
Region of Enrollment
Region of Enrollment(participants)Group 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)Total
United States2132092032092092141257
Smoking frequency
Smoking frequency(Participants)Group 1 (General Snus-Control Ads)Group 2 (General Snus-Multiple Disease Ads)Group 3 (General Snus- Lung Ads)Group 4 (Copenhagen-Control Ads)Group 5 (Copenhagen-Multiple Disease Ads)Group 6 (Copenhagen- Lung Ads)Total
Smoke every day176165161166166164998
Smoke some days374442434350259
08

Study locations

1 site
  • Rutgers Institute for Nicotine & Tobacco Studies
    New Brunswick, New Jersey 08901, United States
09

References and documents

Study documents

  • Protocol and statistical analysis plan · Feb 10, 2026
  • Informed consent form · Apr 3, 2025

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — The study ad stimuli, survey instrument, codebook, and de-identified dataset will be deposited to a data repository - we anticipate this will be the National Addiction and HIV Data Archive Program (NAHDAP), currently managed by ICPSR at the University of Michigan.

Supporting information: Analytic code

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT06927700
Lead sponsor
Rutgers, The State University of New Jersey
Collaborators
National Cancer Institute (NCI)
Responsible party
Olivia A. Wackowski, PhD, MPH (Associate Professor, Rutgers, The State University of New Jersey) — Principal investigator
First posted
Apr 15, 2025
Start date
Apr 24, 2025
Primary completion
May 4, 2025
Completion
May 4, 2025
Results posted
Mar 4, 2026
Last update
Mar 4, 2026

Study contacts

Olivia A Wackowski, PhD, MPH
principal investigator · Rutgers University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion