Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Mustansiriyah University
Baghdad, Bab Al-Moadham, Iraq, 10047
Actively Recruiting
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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