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ACTIVE NOT RECRUITING NA

Effect of Whitening Agent With Emulsion Gel in Saliva and Halitosis

NCT06194123 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this study is to evaluate how well the study product, Crest Daily Whitening Serum, alleviates Xerostomia and perceived halitosis over 1 week of use.

Conditions Studied

Interventions

  • OTHER Crest Daily Whitening Serum

Study Locations (1)

Massachusetts

  • Tufts University School of Dental Medicine — Boston

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2024-02-01
Est. Completion 2027-02-01
Phase NA

Sponsor

Tufts University

78 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06194123

The ClinicalTrials.gov registry entry for NCT06194123 describes a study currently listed as active not recruiting. 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 27 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tufts University, which has 78 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Xerostomia appearing as the primary indexed condition, and to 1 intervention — of which Crest Daily Whitening Serum 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: NCT06194123 reports 1 study location spanning 1 distinct geographic area — top geographies include Massachusetts. 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 NCT06194123 about?

NCT06194123 is a clinical study titled "Effect of Whitening Agent With Emulsion Gel in Saliva and Halitosis". The objective of this study is to evaluate how well the study product, Crest Daily Whitening Serum, alleviates Xerostomia and perceived halitosis over 1 week of use.

What is the current status of trial NCT06194123?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 27 participants. The study started on 2024-02-01. Estimated completion is 2027-02-01.

What conditions does trial NCT06194123 study?

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

What interventions are being tested in trial NCT06194123?

The interventions under investigation include: Crest Daily Whitening Serum (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06194123?

This trial is sponsored by Tufts University, which has 78 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06194123 being conducted?

This trial has 1 study location across Massachusetts. 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