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A clinical trial to study the effects of two light cured indirect pulp capping agents

A randomized controlled clinical trial to compare two light cured indirect pulp capping agents : an in-vivo study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061916
Enrollment
40
Registered
2024-01-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: K029- Dental caries, unspecified

Interventions

Intervention1: Hydrocal LC: Dose- 1g Frequeny of drug administration - once Route of Administration- via syringe over lesion Duration of therapy - around 10 to 15 minutes Control Intervention1: Bine

Sponsors

College of dental sciences and research center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Posterior Teeth having occlusal or proximal deep carious lesion, Healthy periodontium

Exclusion criteria

Exclusion criteria: Teeth with pulp exposure, Sinus opening, Mobility, Cracked tooth

Design outcomes

Primary

MeasureTime frame
To evaluate the pain and tooth sensitivity after treatment long-term outcome of Biner LC over Hydrocal LC as an indirect pulp capping material.Timepoint: The outcome would be assessed at baseline, 1 week,1 month, 3 months and 6 months—

Secondary

MeasureTime frame
To observe whether any periapical lesion is developing or not via radiographs during follow up periodsTimepoint: At 1 week, 3 months & 6 months period during follow up after treatment is provided—

Countries

India

Contacts

Public ContactDr Shilpa Shah

College of Dental sciences and research center

drshah16@gmail.com9376121229

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026