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NCT02309294 · ClinicalTrials.gov registry record · NA

14-Day Cumulative Irritation Patch Test in Subjects With Normal Skin

A NA study, sponsored by Church & Dwight Company.

Completed
Registry status
NA
Development phase
43
Enrollment target

NCT02309294: Completed NA study, sponsored by Church & Dwight Company.

NCT02309294 is a NA study that has completed, run by Church & Dwight Company. The registered enrollment target is 43 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT02309294, a NA study, has completed, sponsored by Church & Dwight Company.

COMPLETED
Registry status
NA
Development phase
43 participants
Enrollment target

Study Summary

The objective of this study is to determine the ability of the study material to cause irritation to the skin of humans under controlled patch test conditions. Substances that come into contact with human skin need to be evaluated for their propensity to irritate and/or sensitize. This testing is a modified primary irritancy patch test that can detect weak irritants that require multiple applications to cause a skin reaction.

Primary Outcome

Score of less than or equal to 1.2 on the Cumulative Irritation Test scale (0-5).

Interventions

  • DEVICE Novel lubricant Miami w/ fragrance
  • DEVICE Novel lubricant Miami no fragrance
  • DEVICE KY Liquid lubricant
  • DEVICE Astroglide Gel lubricant
  • DEVICE Wet Platinum lubricant

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2014-12
Est. Completion 2014-12
Phase NA
Church & Dwight Company

19 total trials

What the finished NCT02309294 record still lists

NCT02309294 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 5 interventions - of which Novel lubricant Miami w/ fragrance is the first listed.

NCT02309294 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02309294 about?

NCT02309294 is a clinical study titled "14-Day Cumulative Irritation Patch Test in Subjects With Normal Skin". The objective of this study is to determine the ability of the study material to cause irritation to the skin of humans under controlled patch test conditions. Substances that come into contact with human skin need to be evaluated for their propensity to irritate and/or sensitize. This testing is a ...

What is the current status of trial NCT02309294?

This trial is currently completed. It is a NA study. The enrollment target is 43 participants. The study started on 2014-12. Estimated completion is 2014-12.

What interventions are being tested in trial NCT02309294?

The interventions under investigation include: Novel lubricant Miami w/ fragrance (DEVICE), Novel lubricant Miami no fragrance (DEVICE), KY Liquid lubricant (DEVICE), Astroglide Gel lubricant (DEVICE), Wet Platinum lubricant (DEVICE).

Who is sponsoring clinical trial NCT02309294?

This trial is sponsored by Church & Dwight Company, which has 19 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02309294's enrollment target sits among peer trials

43 1435th of 2000 higher than 565 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02309294, the US trial registry maintained by the National Library of Medicine. NCT02309294 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.