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OpenTrials
Completed

NCT Number: NCT03047759

Comparison of Two Interdental Cleaners

Comparison of Two interdental cleaning devices on plaque removal, gingivitis and bleeding.

Completed

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Key information

Age range

25 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

This study measured plaque accumulation, bleeding on probing and gingivitis using the Rustogi Modification of the Navy Plaque Index, BOP and Modified Gingival Index at baseline, 2-weeks and 4-weeks.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy adult
  • Non smoker
  • Available for 4-weeks
  • Able to provide written informed consent.
  • Minimum of 20 natural teeth.
  • Minimum requirement for plaque, gingivitis and bleeding.

Exclusion criteria

  • Medical condition
  • No antibiotics within 6 months of study start
  • Not on any medication (impact oral health).

Treatment and study plan

Water Flosser

Device

Powered

air floss

Device

Powered

Primary outcomes

  1. Bleeding upon probing

    Time frame: 4 weeks

    Bleeding upon probing

Secondary outcomes

  1. Gingivitis

    Time frame: 4 weeks

    Modified Gingival \\index

  2. Plaque

    Time frame: 4 weeks

    Rustogi Modification of the Navy Plaque Index

Sponsors and collaborators

Lead sponsor

All Sum Research Center Ltd.

Other

Registry information

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Feb 9, 2017
Registry last updated
Feb 9, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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