Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03237624 · ClinicalTrials.gov registry record · NA

Functional Chewing Gum in Reduction of Gingival Inflammation

A NA study, sponsored by University of Maryland, Baltimore.

Completed
Registry status
NA
Development phase
34
Enrollment target

NCT03237624: Completed NA study, sponsored by University of Maryland, Baltimore.

NCT03237624 is a NA study that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 34 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03237624, a NA study, has completed, sponsored by University of Maryland, Baltimore.

COMPLETED
Registry status
NA
Development phase
34 participants
Enrollment target

Study Summary

The aim of this prospective randomized 3-month double-blinded single center study is to determine whether a chewing gum device with food additive chitosan, will aid in reducing gingival inflammation by supplementing traditional tooth brushing and flossing measures. Patients with mild to moderate gingivitis will be identified and enrolled in this investigation. All enrolled subjects will receive baseline oral hygiene brushing instructions and a baseline clinical examination of the gingiva. The test group will utilize the test chewing gum three times a day for a minimum 20-30 minutes duration; the control group will receive a placebo gum and use it in a similar manner. We will examine whether daily use of a functional chewing gum enhances improvements to brushing and flossing.

Primary Outcome

Measure the color of gingiva - use Gingiva Index

Interventions

  • DEVICE Functional Chitosan Chewing Gum
  • DEVICE Control Chewing Gum
  • BEHAVIORAL Oral hygiene measures

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2018-01-31
Est. Completion 2020-01-31
Phase NA
University of Maryland, Baltimore

560 total trials

What the finished NCT03237624 record still lists

NCT03237624 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 3 interventions - of which Functional Chitosan Chewing Gum is the first listed.

NCT03237624 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03237624 about?

NCT03237624 is a clinical study titled "Functional Chewing Gum in Reduction of Gingival Inflammation". The aim of this prospective randomized 3-month double-blinded single center study is to determine whether a chewing gum device with food additive chitosan, will aid in reducing gingival inflammation by supplementing traditional tooth brushing and flossing measures. Patients with mild to moderate gin...

What is the current status of trial NCT03237624?

This trial is currently completed. It is a NA study. The enrollment target is 34 participants. The study started on 2018-01-31. Estimated completion is 2020-01-31.

What interventions are being tested in trial NCT03237624?

The interventions under investigation include: Functional Chitosan Chewing Gum (DEVICE), Control Chewing Gum (DEVICE), Oral hygiene measures (BEHAVIORAL).

Who is sponsoring clinical trial NCT03237624?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03237624's enrollment target sits among peer trials

34 1570th of 2000 higher than 427 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02897063 · 34 participants · Phase 1

    Effects of Midodrine and Droxidopa on Splanchnic Capacitance in Autonomic Failure

  • NCT03906617 · 34 participants · Phase 4

    Bupivacaine/Epinephrine +Dexamethasone vs. Liposomal Bupivacaine

  • NCT03992378 · 34 participants · NA

    Neuromodulation to Regulate Inflammation and Autonomic Imbalance in Sepsis

  • NCT04047849 · 34 participants · Phase 4

    Latency Antibiotics in Previable PPROM, 18 0/7- 22 6/7 WGA

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03237624, the US trial registry maintained by the National Library of Medicine. NCT03237624 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.