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Comparing New and Traditional Dental Materials to Protect Children s Back Teeth During Treatment

COMPARATIVE EVALUATION OF THERACAL LC NEOPUTTY MTA AND CONVENTIONAL MTA FOR INDIRECT PULP CAPPING IPC TREATMENT IN PRIMARY MOLARS A PROSPECTIVE RANDOMIZED CONTROLLED STUDY - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094832
Enrollment
108
Registered
2025-09-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: K025- Dental caries on pit and fissure surface

Interventions

Intervention1: Theracal lc: application of rubber dam then removal of caries cleaning the cavity properly then applying theracal LC as pulp capping material followed by GIC restoration Intervention2:

Sponsors

Shagun Rana
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Paediatric patients rated as definitely positive Frankl Score 4 or positive Frankl Score 3 on the Frankl Behaviour Rating Scale 2 Pediatric patients with a history of dull reversible pain or mild discomfort during chewing 3 Patients with at least one restorable primary first or second molar on either side of the mouth with an occlusal cavitated active carious lesion involving more than fifty percent of dentin thickness as confirmed radiographically 4. Teeth with no clinical signs of spontaneous pain or tenderness on percussion 5. Parents or guardians who provide written informed consent for their childs participation in the study

Exclusion criteria

Exclusion criteria: 1 Teeth with clinical signs of abscess fistula or swelling 2 Teeth exhibiting signs of inflammation such as abnormal mobility tenderness to percussion or palpation or spontaneous pain 3. Teeth with radiographic evidence of apical or furcal lesions or pathological root resorption 4. Children with metabolic disorders systemic illnesses or medically compromised conditions that may influence the study outcomes 5. Children or parents or guardians who do not consent to participation in the study

Design outcomes

Primary

MeasureTime frame
1Clinical and Radiographic Success 2Remaining Dentin Thickness (CBCT) Timepoint: Clinical and radiographic data will be collected at T0 baseline T1 6 months and T2 12 months CBCT scans will be done at immediate post operatively and T2 12 months

Secondary

MeasureTime frame
1 Clinician Ease of Handling 2 Adverse Reactions Timepoint: Immediate post operative T1 6 months T2 12 months

Countries

India

Contacts

Public ContactDr Afroz Alam ansari

Faculty of dental science KGMU Lucknow

afrozalamansari@rediffmail.com9335166662

Outcome results

None listed

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