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This study aimed to assess and compare the clinical and radiographic success rates of LLLT and FC for pulpotomy in human primary teeth. One hundred and six primary molars from 36 children aging five to eight years were included and randomly assigned into two equal groups; LLLT group and FC group. Teeth were evaluated clinically and radiographically at 3, 6 and 12 months.
Background: Various agents are available to dress the remaining pulp tissue after pulpotomy procedure with the formocresol (FC) being the gold standard for the last 60 years. Nowadays, low-level laser therapy (LLLT) becomes a technique of interest, due to its many characteristics. However, the literature available on its success in pulpotomy is limited and reported conflicting results.
Aim of the study: To assess and compare the clinical and radiographic success rates of LLLT and FC for pulpotomy in human primary teeth.
Materials and methods: Utilizing split-mouth technique, the sample consisted of 106 primary molars from 36 children aging five to eight years. The teeth were selected based on specific clinical and radiographic inclusion criteria and randomly assigned into two equal groups; LLLT group and FC group. All the 106 primary molars were indicated for pulpotomy, where 53 teeth were treated using FC and 53 teeth were treated with LLLT. Teeth were evaluated clinically and radiographically at 3, 6 and 12 months.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Low-level laser therapy group | Experimental | This group of teeth received laser irradiation after amputation of coronal pulp |
|
| Formocresol group | No Intervention | This group of teeth received the gold standard medication (formocresol) after coronal pulp amputation |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Low-level laser therapy | Device | It is a diode laser device that has laser set at low level, used for pain relief and inflammation reduction to induce healing |
|
| Measure | Description | Time Frame |
|---|---|---|
| Clinical success rate | The pulpotomy procedure was considered clinically successful if there were no pain, swelling, tenderness to percussion, abscess or abnormal mobility | 3 months |
| Clinical success rate | The pulpotomy procedure was considered clinically successful if there were no pain, swelling, tenderness to percussion, abscess or abnormal mobility | 6 months |
| Clinical success rate | The pulpotomy procedure was considered clinically successful if there were no pain, swelling, tenderness to percussion, abscess or abnormal mobility | 12 months |
| Radiographic success rate | The pulpotomy procedure was considered clinically successful if it demonstrated the following criteria:
| 3 months |
| Radiographic success rate | The pulpotomy procedure was considered clinically successful if it demonstrated the following criteria:
| 6 months |
| Radiographic success rate | The pulpotomy procedure was considered clinically successful if it demonstrated the following criteria:
| 12 months |
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Inclusion Criteria:
Children inclusion criteria:
Teeth inclusion criteria:
Teeth were selected according to clinical and radiographic criteria.
Clinically, the study included:
Radiographically, the recruited teeth should have:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| King Abdulaziz University, Dental University Hospital | Jeddah | 21589 | Saudi Arabia |
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| ID | Term |
|---|---|
| D028022 | Low-Level Light Therapy |
| ID | Term |
|---|---|
| D053685 | Laser Therapy |
| D013812 | Therapeutics |
| D010789 | Phototherapy |
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It is a split-mouth randomized controlled clinical trial
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