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Clinical trial to evaluate the success rate of indirect pulp capping procedure with four pulp capping materials in permanent teeth - a randomized clinical trial

Evaluation of success rate of indirect pulp capping procedure with mineral trioxide aggregate, biodenntine and calcium hydroxide in permanent teeth

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/044347
Enrollment
100
Registered
2022-07-26
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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: biodentine: Biodentine, Septodont Intervention2: mineral trioxide aggregate: MTA Angelus® Reparative Cement Control Intervention1: calcium hydroxide: Dentsply Dycal Radiopaque Calcium

Sponsors

thilothamma k
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age group 18 â?? 40 years Tooth with deep caries,no pain,no periapical and periodontal lesions Positive pulpal response

Exclusion criteria

Exclusion criteria: History of systemic diseases Clinical and radiographic evidences of pulpal involvement associated with no spontaneous or nocturnal pain, no tenderness on percussion and no periodontal diseases Uncontrollable pulpal bleeding

Design outcomes

Primary

MeasureTime frame
no pain or sensitivity, positive tertiary dentin formation, no periapical radiolucencyTimepoint: no pain or sensitivity, positive tertiary dentin formation, no periapical radiolucency at baseline, 3 months and 6 months—

Secondary

MeasureTime frame
nilTimepoint: nil—

Countries

India

Contacts

Public ContactDr Thilothamma K

Karpaga vinayaga institute of dental sciences

ashokleburumds@gmail.com9884145541

Outcome results

None listed

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