← Back to all trials
Completed
NCT05680285
Evaluation of Low Level Laser Therapy in Primary Tooth Pulpotomy Treatment
Conditions: Pulpotomy
Sex: All
Ages: 6 Years – 9 Years
Healthy volunteers: 1
Phase: NA
Enrollment: 90
Sponsor: Uşak University
Location: Turkey
Summary
In our study, it was aimed to compare the long-term effectiveness of diode laser and low level laser therapy and primary tooth amputation treatments using calcium hydroxide (LLLT+CH) in primary second molars with deep dentinal caries.
Ninety patients ( 42 Gırl, 48 Boy) aged 6-9 years with deep dentin caries in the mandibular second molar were included in the study.
The patients were randomly selected according to the treatment to be applied and divided into two groups as the diode laser group (N=45) and the LLLT+CH group (N=45).
The patients were called for control appointments at the 1st, 3rd, 6th and 12th months after the treatment, and both clinical and radiographic follow-ups were performed.
Chi-square and Fisher's Exact tests were used to compare categorical variables according to groups in statistical analysis, and p<0.05 was considered significant.
When the study results at the end of 12 months were evaluated, the diode laser group had a clinical success rate of 95.6%, and a success rate of 93.3% radiologically; The LLLT+CH group had a success rate of 97.7% clinically and 90.9% radiologically.
There was no statistically significant difference between the success rates of the groups (p>0.05).
According to the clinical and radiographic results of our study, it was determined that diode laser and LLLT+CH amputations showed similar success rates in primary second molars with deep dentin caries.
It has been seen that both methods can be used safely in primary tooth amputations.
It is thought that clinical and histological studies and studies examining the effectiveness of dental laser applications in primary tooth amputation treatment are needed.
Eligibility Criteria
Inclusion Criteria:Clinical CriteriaNo systemic diseaseNot allergic to the materials usedChildren with scores of 1 and 2 according to the Frankel behavioral scaleThose who have erupted permanent first molarsThe one in occlusion with the opposing toothNot having bad oral habitsNo structural anomaly in the teethNo spontaneous or nocturnal painNo sensitivity to palpation or percussionAbscess and fistula formation freeNo pathological mobilityDuring treatment, pulp bleeding is controlled within 5 minutes.With a crown that can be made of stainless steel crown (PÇK)Radiographic CriteriaHaving a deep dentin caries lesion very close to the pulpNo resorption in the bifurcation and periapical areaPeriodontal space is healthy and there is no periapical region pathologyAbsence of internal and external root resorption in rootsNo calcified masses in the pulpTeeth that did not exceed one-third of the physiological root resorption were included in the study.Exclusion Criteria-Children with a score of 1 and 4 on the Frankel Scale were excluded.
Source: ClinicalTrials.gov (NCT05680285). StuddyBuddy aggregates publicly available trial information.