Skip to content

Clinical and X-ray Evaluation of Three Different Materials for Treating Tooth Decay in Primary Molars: A Study in Children

Clinical and Radiographic Evaluation Of Three Different Indirect Pulp capping Materials in Primary Molars: A Randomized Clinical study - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/074844
Enrollment
79
Registered
2024-10-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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: EndoSequence root repair material (ERRM): EndoSequence root repair material (ERRM) is a calcium silicate based cement, available in premixed putty form. Dose/Quantity: Sufficient amount

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Cooperative patients with FRANKL rating 3 and 4. 2.Restorable first or second primary molar (maxillary or mandibular molar) with deep occlusal carious lesions involving approximately 3/4th of the dentin. 3.Teeth with signs of reversible pulpitis 4.No history of spontaneous pain, tenderness to percussion, abscess or fistula. 5.Absence of clinical and radiographical pulp involvement 6.Extension of caries such that it has potential to expose the pulp if removed completely 7.Teeth with the absence of pathological root resorption or periapical or furcal radiolucency 8.Teeth with less than one-third physiological root resorption

Exclusion criteria

Exclusion criteria: 1.Medically compromised patients 2.Uncooperative patients with FRANKL scale less than 3 3.Teeth with history of night pain, abscess, swelling and tenderness. 4.Teeth with clinical or radiographic involvement of pulp 5.Teeth with periapical or furcal radiolucency 6.Patients who decline to participate

Design outcomes

Primary

MeasureTime frame
Preservation of pulp vitality assessed through clinical and radiographic evaluations (absence of symptoms such as pain, swelling, or signs of infection, and no radiographic evidence of periapical pathology or internal resorption post operative pain (VAS) Timepoint: 3, 6, 9, 12 months

Secondary

MeasureTime frame
Restorative material integrity (USPHS criteria) Timepoint: 3, 6, 9, 12 months

Countries

India

Contacts

Public ContactBhawana Kumari

KING GEORGES MEDICAL UNIVERSITY

rajkids2000@yahoo.co.in9450849528

Outcome results

None listed

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