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A Comparative In Vivo Study of clinical and radiographic outcomes of pulpotomy of permanent posterior teeth with carious pulp exposure using only Bioceramic material and applying LASER before using Bioceramic material

Comparative evaluation of clinical and radiographic outcomes of pulpotomy of permanent posterior teeth with carious pulpal exposure using only Bioceramic material and applying LASER before using Bioceramic material : An In Vivo Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112049
Enrollment
36
Registered
2026-06-05
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K040- Pulpitis

Interventions

Intervention1: Complete coronal pulpotomy: Pulpotomy with application of Diode LASER before using Bioceramic material (Biodentine, Septodont) Intervention2: Complete coronal pulpotomy: Pulpotomy using

Sponsors

Guru Nanak Institute of Dental Sciences and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Mature permanent molar tooth (with signs and symptoms of either symptomatic irreversible pulpitis or asymptomatic carious lesion with pulp exposure or reversible pulpitis with pulp exposure where hemostasis is not readily controlled and pulpal tissue appear normal) with restorable deep class I caries involving the pulp .

Exclusion criteria

Exclusion criteria: Tooth with large carious lesion which cannot be restored with direct filling materials. On removal of pulpal tissue till orifice level if hemostasis is not achieved readily. Pregnant or lactating mothers. Patients with serious systemic health diseases. Tooth with tenderness or mobility. Tooth with reversible pulpitis, crack, cusp fracture, subgingival caries

Design outcomes

Primary

MeasureTime frame
The outcome of pulpotomy using Bioceramic material without LASER and with LASER will be evaluated clinically and radiographically. Follow ups will be done at 7 days, 1 month and 3 months to evaluate postoperative pain, swelling and tenderness on percussion as well as radiographically to check for dentinal bridge formation, root resorption and periapical radiolucency at 1 and 3 months. So the expected outcome will be variations in evaluation in the outcomes between two groups.Timepoint: Follow ups will be done after 24 hours, 1 week, 1 month and 3 month

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Katha Mandal

Guru Nanak Institute of Dental Sciences and Research

kathamandalkm@gmail.com7327899734

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026