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临床试验/ISRCTN66780304
ISRCTN66780304已完成不适用

ong-term use of combination oral hygiene on gingival and periodontal health: a pilot study

Procter & Gamble0 个研究点目标入组 110 人开始时间: 2018年5月11日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
110

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Give written informed consent and receive a copy of their consent
  • 2. Be between the ages of 18 and 65
  • 3. Be in good general health as determined by the Investigator/designee based on a review of the medical history/update for participation in the study
  • 4. Possess a minimum of 16 natural teeth (excluding third molars) with facial and lingual scorable surfaces
  • 5. Have at least 20 bleeding sites (sum of sites with a score of 1 or 2 on the GBI index)
  • 6. Have at least: 3 eligible healthy sites (PPD <3 mm, no bleeding), 3 eligible gingivitis sites (PPD < 3 mm, bleeding), and 3 eligible periodontal sites (PPD 3-6 mm, bleeding)
  • 7. Agree to delay any elective dentistry until study completion, including additional dental prophylaxes outside the study protocol
  • 8. Agree to refrain from using any non-study oral hygiene products for the study duration (subject will be allowed to continue using floss but they will be instructed not to add/change any other oral hygiene products, including whitening products etc)
  • 9. Agree not to participate in any other oral care clinical study for the duration of this study
  • 10. Agree to return for their scheduled visits and follow study procedures

排除标准

  • 1. Severe periodontal disease, as characterized by purulent exudate, generalized mobility, and/or severe recession
  • 2. Active treatment for periodontitis
  • 3. Having a medical condition requiring antibiotic pre-medication prior to dental procedures
  • 4. Fixed facial or lingual orthodontic appliances or removable partial dentures
  • 5. Antibiotic or chlorhexidine use or anti-inflammatory medications within two weeks prior to Screening visit
  • 6. Self-report nursing, pregnancy, or intent to become pregnant during the study
  • 7. Dental prophylaxis within two months prior to the Screening visit
  • 8. Any diseases or conditions that could be expected to interfere with the subject safely completing the study

研究者

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