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NCT02641912 · ClinicalTrials.gov registry record · NA

Potential of an Experimental Mouthwash Formulation to Reduce Dry Mouth Symptoms

A NA study of Xerostomia, sponsored by GlaxoSmithKline.

Completed
Registry status
NA
Development phase
100
Enrollment target
1
Study location

NCT02641912 is a NA study of Xerostomia that has completed, run by GlaxoSmithKline. The registered enrollment target is 100 participants, above the 88-participant average among 13 other Xerostomia trials with a reported enrollment target (14% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT02641912, a NA study of Xerostomia, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
NA
Development phase
100 participants
Enrollment target
1
Study location

Study Summary

This will be a single center, 7-day, examiner blind, two treatment-arm, randomized, stratified (Sjogren's Syndrome status \[Y/N\]), parallel group study conducted in participants experiencing dry mouth symptoms. This study is designed to investigate the effect of an experimental mouthwash formulation in providing relief of dry mouth symptoms.

Conditions Studied

Interventions

  • OTHER Biotene mouthwash
  • OTHER Mineral Water

Study Locations (1)

Massachusetts

  • GSK Investigational Site - Boston

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2016-03-09
Est. Completion 2016-04-15
Phase NA

Sponsor

GlaxoSmithKline

1,345 total trials

What the Registry Record Tells You About NCT02641912

The ClinicalTrials.gov registry entry for NCT02641912 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 88-participant average among 13 other Xerostomia trials with a reported enrollment target (14% higher). The listed sponsor is GlaxoSmithKline, which has 1,345 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Xerostomia appearing as the primary indexed condition, and to 2 interventions - of which Biotene mouthwash is the first listed.

NCT02641912 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT02641912 about?

NCT02641912 is a clinical study titled "Potential of an Experimental Mouthwash Formulation to Reduce Dry Mouth Symptoms". This will be a single center, 7-day, examiner blind, two treatment-arm, randomized, stratified (Sjogren's Syndrome status \[Y/N\]), parallel group study conducted in participants experiencing dry mouth symptoms. This study is designed to investigate the effect of an experimental mouthwash formulatio...

What is the current status of trial NCT02641912?

This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2016-03-09. Estimated completion is 2016-04-15.

What conditions does trial NCT02641912 study?

This clinical trial studies the following conditions: Xerostomia.

What interventions are being tested in trial NCT02641912?

The interventions under investigation include: Biotene mouthwash (OTHER), Mineral Water (OTHER).

Who is sponsoring clinical trial NCT02641912?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02641912 being conducted?

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

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

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