Periodontitis Clinical Trial
Official title:
The Effect of Locally Delivered Ciclosporin as an Adjunct to Healing After Treatment of Periodontal Pockets
Verified date | April 2017 |
Source | PerioC Limited |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main purpose of the trial is to investigate the effect of locally delivered ciclosporin as an adjunct to non-surgical mechanical debridement in the treatment of chronic periodontitis and to compare it to mechanical debridement alone.
Status | Completed |
Enrollment | 23 |
Est. completion date | October 2016 |
Est. primary completion date | September 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Years and older |
Eligibility |
Inclusion Criteria: - Patients in good general health - 2 pairs of contralateral interproximal periodontal sites with probing depths of =7mm in single-rooted teeth not associated with furcations or root furrows.The test sites should have a distance of at least two teeth to the control sites. - Teeth selected should have a vital pulp as determined by thermal or electric stimulation Exclusion Criteria: - Patients already included in other clinical trials involving therapeutic intervention (either medical or dental) - Periodontal treatment during the last 6 months - Antibiotic treatment 6 months prior to the start of the trial - Antibiotic prophylaxis required for dental treatment - Patients with acute infectious lesions in the areas of intended treatment - Regular anti-inflammatory medication - Known history of ciclosporin allergy - Ongoing medication that may affect the clinical features of periodontitis - Patients who are smokers - Patients that are immuno-compromized or on immunosuppressive medication - Patients who are pregnant or lactating |
Country | Name | City | State |
---|---|---|---|
Sweden | The Sahlgrenska Academy, University of Gothenburg | Gothenburg |
Lead Sponsor | Collaborator |
---|---|
PerioC Limited |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Probing pocket depth (PPD) | Mean change in probing pocket depth (PPD) from baseline to 3-month examination | 3 months | |
Primary | Bleeding on Probing (BoP) | Change in BoP (measured as present or absent) from baseline to 3-month examination | 3 months |
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