Actively Recruiting

Phase 3
Age: 20Years - 24Years
All Genders
Healthy Volunteers
NCT06882564

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

Led by Al-Mustansiriyah University · Updated on 2025-03-18

54

Participants Needed

1

Research Sites

42 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 20Years - 24Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Organoleptic tongue score greater than 2 on a 0-5 scale
  • Male or female undergraduate dental students without chemical plaque control measures for at least one week
  • Students with halitosis due to gingivitis
  • Age between 20 and 23 years
  • No periodontal treatment for at least one month
  • No systemic disease
  • Non-smokers
  • At least 20 teeth present
Not Eligible

You will not qualify if you...

  • Smokers and alcoholics
  • Patients with periodontitis or pocket depth greater than 6 mm
  • Patients with orthodontic appliances
  • Presence of open carious lesions, pericoronitis, dry socket, or fistula
  • Patients with systemic diseases or conditions
  • Taking medication within the last two weeks
  • Consumed garlic, onion, or licorice in the last 24 hours
  • Used oral hygiene products in the last 24 hours
  • Pregnant women
  • Sinusitis, tonsillitis, or upper respiratory tract infection

AI-Screening

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Trial Site Locations

Total: 1 location

1

Mustansiriyah University

Baghdad, Bab Al-Moadham, Iraq, 10047

Actively Recruiting

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Research Team

N

NOOR AA TAHER, B.D.S

CONTACT

N

NOOR AA TAHER, B.D.S

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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