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A study to evaluate pain relief and tooth health after Biodentine treatment in sensitive worn-down back teeth.

Evaluation of Biodentine Pulpotomy of Attrited Sensitive Molars: A One-Year Clinical Follow-Up - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104528
Enrollment
80
Registered
2026-02-23
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: K030- Excessive attrition of teeth

Interventions

Intervention1: Biodentine: Septodont Healthcare India Pvt. Ltd. Maharashtra, India LOCAL DRUG DELIVERY: Equal proportions of powder and liquid of Biodentine are mixed using a spatula under an oil imp

Sponsors

Denesh P.S.G
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of age 30 - 70 years Mild to moderate sensitivity (Schiff cold air sensitivity scale) Maximum of 3 such attrited teeth in a patient No history of management of such teeth Teeth with No pulpal calcifications

Exclusion criteria

Exclusion criteria: Patient with any systemic ailments patients with symptoms of irreversible pulpitis patients who cant localise pain patient who are immunocompromised and under medication Pregnant women Patient who are not willing to undergo the treatment Teeth that cannot be saved through root canal treatment

Design outcomes

Primary

MeasureTime frame
Assessment of post - operative pain after Biodentine pulpotomyTimepoint: 24 hours, 48 hours.—

Secondary

MeasureTime frame
Assessment of tooth survival following Biodentine pulpotomyTimepoint: 6 months, 12 months.—

Countries

India

Contacts

Public ContactDr I Anand Sherwood

CSI college of dental sciences and research

anand.sherwood@gmail.com9443805150

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026