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Periodontal Disease Treatment of a Physically Challenged Population (PDT)

O

Oravital

Status

Completed

Conditions

Periodontal Disease

Treatments

Drug: metronidazole-nystatin oral rinse

Study type

Interventional

Funder types

Industry

Identifiers

NCT01718912
TRI (Other Identifier)
OVTRI

Details and patient eligibility

About

Many physically handicapped patients at the dental department, Toronto Rehabilitation Institute(TRI) have considerable gingival inflammation and breath odour because of the inability to effectively handle a toothbrush. These patients have considerable periodontal disease. There is a concern that these pathogens may have a detrimental effect on wound healing in other areas of the body.

Hypothesis: Patients attending the dental department at TRI that are treated with the antibiotic-antifungal rinse containing metronidazole and nystatin will show substantial decrease in periodontal disease as measured by bleeding points and pocket depth when compared to the group that continues to use their regular oral hygiene methods (control group).

Enrollment

11 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Participants must be between the ages of 18 to 65 years Participants must have at least 6 teeth. Participants must have some indication of gingivitis and periodontal breakdown. -

Exclusion criteria

Patients who are taking Warfarin/Coumadin Patients who are allergic to Metronidazole or chlorhexidine. Edentulous patients will be excluded by those who have at least 6 teeth can be a participant

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

11 participants in 1 patient group

Metronidazole-nystatin oral rinse, regular oral hygiene
Other group
Description:
Week 1: daily brushing with suction brush. Week two: daily brushing with a mixture of metronidazole-nystatin suspension.
Treatment:
Drug: metronidazole-nystatin oral rinse

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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