Last updated 18 months ago

Effectiveness of Photodynamic Therapy in the Disinfection of Root Canals in Patients With Apical Lesion

159 patients around the world
Available in Chile
The object of the present study is to compare the effectiveness of conventional endodontic treatment with that of endodontic treatment combined with PDT in patients with apical lesion. A randomized, clinical, superiority trial will be carried out, controlled, blinded and masked, with 3 parallel arms. The patient sample will be randomized in 3 treatment groups: the first is the placebo group which will receive conventional endodontic treatment (ET) and a simulated treatment with the equipment in which no radiation will be emitted; the second group will receive conventional ET associated with PDT with diode laser at 660 nm, fluence 10 s/canal; and the third group will receive conventional ET associated with PDAT with laser at 660 nm, 20 s/canal. The photosensitizer used in the PDT will be methylene blue. Clinical and radiographic examination of all the patients will be used to obtain baseline values (T0) and values 6 months post-treatment (T1). The presence and size of apical lesion will be assessed at T0 and T1, the percentage reduction of the lesion will be calculated and the PAI index will be used as a scoring system to assess the lesion. The success rate will be assessed for each group 6 months after completion of the treatment. Disinfection of the root canals will be assessed by analysis of colony formation (ufc/ml); biological samples will be taken with paper cones inserted into the root canals to the apical region at two moments: Baseline (before treatment, T0); after instrumentation with PDT (experimental groups) and without PDT (placebo group). Adverse events will be analysed; a serious adverse event for this study is any unfavourable odontological event that the investigators believe to bear a causal relation with the experimental intervention.
Universidad de La Frontera
1Research sites
159Patients around the world

Requirements for the patient

To 80 Years
All Gender

Medical requirements

Patients eligible for this study must comply with the following for randomization: 1. Adult patients of either sex 2. No general biological risk 3. At least 1 molar with pulp necrosis and apical lesion
Pregnancy
Patients requiring complex dental rehabilitation due to major coronal destruction
Individuals with cognitive disability making conventional treatment impossible

Sites

UNIVERSIDAD SAN SEBASTIÁN, FACULTAD DE MEDICINA Y CIENCIA
Recruiting
Providencia, Región Metropolitana de Santiago 7500000
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