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NCT06882564RecruitingPhase 3

Efficacy of Resveratrol Containing Mouthwash in Reducing Halitosis Related Porphyrymonas Gingivalis.

Efficacy of Resveratrol Containing Mouthwash in Reducing Halitosis Related Porphyromonas Gingivalis: A Randomized, Triple-blind Clinical Trial

Source: ClinicalTrials.gov · Last updated 18 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The aim of the study: To assess the efficacy of antioxidant (resveratrol) mouthwash in reducing the level of p. gingivitis and oral malodor over 7 day period among undergraduate dental student patients from Mustansiriyah University/College of Dentistry and Wasit University /College of Dentistry. Objectives: * To assess the efficacy of anti-oxidant and anti-inflammatory resveratrol mouthwash in reducing halitosis in undergraduate students with plaque-induced gingivitis patients. * To assess the efficacy of resveratrol mouthwash in reducing p. gingivalis in undergraduate students' patients with oral malodor. * To determine the relation between p.gingivalis and clinical periodontal parameters (plaque index, gingival index, bleeding on probing) among undergraduate students with plaque-induced gingivitis and halitosis.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
54 (estimated)
First submitted
11 Mar 2025
Start date
5 Jan 2025
Primary completion date
1 Apr 2025
Lead sponsor
Al-Mustansiriyah University
NCT number
NCT06882564

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 54
  • From 5 Jan 2025 to the primary completion date, 1 Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • taking medication in the last two weeks

Other illness

  • Open carious lesions, pericoronitis, dry socket, and fistula.
  • Patients with systemic disease and condition
  • sinusitis, tonsilitis, and upper respiratory tract infection

Other

  • Smokers and alcoholics
  • Patient with periodontitis or pocket depth \> 6mm
  • Patient with orthodontics appliance
  • Take garlic, onion, or licorice in the last 24 hours
  • using oral hygiene products in the last 24 hours
  • pregnant women

Who the study is looking for

  • Organoleptic tongue of scores \> 2 using (0-5scale) (Rosenberg and McCulloch, 1992)
  • Male and female undergraduate dental students without chemical plaque control measures for at least one weak
  • Male and female students with halitosis due to gingivitis
  • The age of students ranges from 20 to 23 years.
  • No periodontal treatment for at least one month
  • No systemic disease
  • No tobacco smoking
  • The patients must have at least 20 teeth

Age in the registry: 20 years to 24 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mustansiriyah University
Coordinator of this site? Confirm its status
BaghdadIraqRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.