Health Condition 1: K040- Pulpitis
Conditions
Interventions
Intervention1: MEDICAL DEVICE - iLase - Diode Laser system
Manufacturing company - BIOLASE Inc, USA
: The LASER is activated at a wavelength of 940nm and 0.5W power for 4 seconds on each root canal
Sponsors
Dr R Jesanth Joel
Eligibility
Inclusion criteria
Inclusion criteria: Patients with posterior teeth having spontaneous sensitivity or sensitivity to heat/cold Teeth with reversible pulpitis, that shows immediate sensitive response which subsides on withdrawal of stimulus on cold test. Teeth with no PDL widening or loss of lamina dura on radiographs. Teeth that shows no tenderness to percussion
Exclusion criteria
Exclusion criteria: Teeth where pulpal bleeding prolonging more than 10 mins. Teeth with lingering response on cold test. Patient who are not willing for pulpotomy. Patients having TMJ disorders, calcified canals or periodontally compromised tooth.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the clinical success rates of LASER assisted pulpotomyTimepoint: 3 months, 6 months and 1 year after pulpotomy | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessing the survival of toot after pulpotomy in both the groups.Timepoint: 1 year | — |
Countries
India
Contacts
Public ContactDr S Swathi Priyadharshini
CSI college of dental sciences and research
Outcome results
None listed