None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Healthy male and non-pregnant female 2.Aged between 18 and 65 years. 3.Willing to give signed written informed consent 4.Subjects having AmrÄ?d al-AsnÄ?n (disease of the teeth) with or without any of the following symptoms: a.Bakhr al-Fam (halitosis) b.Quruh al-Litha (gingival ulcer) c.Taharruk al-Asnan (odontoseisis) d.Waram al-Lissa (gingival swelling) e.Humra al-Lissa (gingival erythema) f.Nazf al-Lisa (gingival bleeding) g.Dhahab Maâ?? al-Asnan (sensitive teeth) h.Wajaâ?? al-AsnÄ?n (toothache)
Exclusion criteria
Exclusion criteria: Requirement for prophylactic antibiotic medication, 1.Unable to comply with a study schedule, 2.Untreated caries 3.Periodontitis requiring prompt treatment or 4.Emergency dental treatment, 5.Wearing any kind of oral appliance, 6.History of known allergies 7.Known case of Hemophilia, Low platelet count (thrombocytopenia) and von Willebrand disease (VWD), etc. 8.Known cases of any other acute illness. 9.Known cases of systemic disorders requiring prolonged treatment. 10.Pregnant and lactating women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety of the patientsTimepoint: 14th day, 28th day | — |
Secondary
| Measure | Time frame |
|---|---|
| Efficacy of the toothpaste, VAS scoreTimepoint: 14th day, 28th day | — |
Countries
India
Contacts
NRIUMSD