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COMPLETED NA

A Clinical Study to Assess the Effects of Various Dentifrice Technologies on Dentinal Hypersensitivity

NCT03965039 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this study is to evaluate the efficacy (changes in dentinal hypersensitivity) and safety (oral soft tissue evaluation) after use of one of four dentifrices in subjects with pre-existing hypersensitivity over an 11-week period.

Conditions Studied

Interventions

  • DEVICE Dipotassium oxalate toothpaste
  • DRUG Stannous fluoride toothpaste
  • DRUG Potassium nitrate toothpaste
  • DRUG Sodium monofluorophosphate toothpaste

Study Locations (1)

Nevada

  • Silverstone Research Group — Las Vegas

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2019-07-08
Est. Completion 2019-10-03
Phase NA

Sponsor

Procter and Gamble

25 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03965039

The ClinicalTrials.gov registry entry for NCT03965039 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Procter and Gamble, which has 25 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Dentin Hypersensitivity appearing as the primary indexed condition, and to 4 interventions — of which Dipotassium oxalate toothpaste is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03965039 reports 1 study location spanning 1 distinct geographic area — top geographies include Nevada. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03965039 about?

NCT03965039 is a clinical study titled "A Clinical Study to Assess the Effects of Various Dentifrice Technologies on Dentinal Hypersensitivity". The objective of this study is to evaluate the efficacy (changes in dentinal hypersensitivity) and safety (oral soft tissue evaluation) after use of one of four dentifrices in subjects with pre-existing hypersensitivity over an 11-week period.

What is the current status of trial NCT03965039?

This trial is currently completed. It is a NA study. The enrollment target is 120 participants. The study started on 2019-07-08. Estimated completion is 2019-10-03.

What conditions does trial NCT03965039 study?

This clinical trial studies the following conditions: Dentin Hypersensitivity. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03965039?

The interventions under investigation include: Dipotassium oxalate toothpaste (DEVICE), Stannous fluoride toothpaste (DRUG), Potassium nitrate toothpaste (DRUG), Sodium monofluorophosphate toothpaste (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03965039?

This trial is sponsored by Procter and Gamble, which has 25 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03965039 being conducted?

This trial has 1 study location across Nevada. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial