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