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Comparison of the success of vital pulp therapy using BIODENTINE and Mineral Trioxide Aggregate (MTA)

Investigation the success rate of vital pulp therapy using BIODENTINE in comparison with Mineral Trioxide Aggregate (MTA) in patients referring to a private office in Ilam city

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250615066197N1
Enrollment
46
Registered
2025-07-13
Start date
2025-07-23
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Irreversible Pulpitis. Pulpitis

Interventions

Intervention 1: Intervention group: Under treatment with Biodentine, Biodentine capsule is prepared by gentle tapping and 5 drops of liquid are added to the powder and the capsule is triturated for 30

Sponsors

Ilam University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 15 Years

Inclusion criteria

Inclusion criteria: Patients with immature teeth and incomplete apex The selected tooth should have lost more than one-third of its marginal edge due to caries and be free of abscesses or intraoral sinuses. The tooth should be restorable and there should be no deep dentinal caries near the pulp or iatrogenic pulp exposure Diagnosis of irreversible pulpitis for the tooth and blood in the pulp chamber should be bright red during collection and bleeding should stop within 5-10 minutes after application of cotton soaked in sodium hypochlorite. Radiographic criteria: No evidence of internal or external inflammatory resorption of the roots No evidence of interradicular bone resorption or radiolucency in the root furcation. No evidence of sinus tract

Exclusion criteria

Exclusion criteria: Necrotic teeth Teeth with closed apex primary teeth

Design outcomes

Primary

MeasureTime frame
Clinical success. Timepoint: 3, 6 and 9 months after Vital Pulp Therapy. Method of measurement: Clinical success will be determined by the absence of pain, tenderness, inflammatory swelling, mobility, and the presence of a fistula or sinus.;Radiographic success. Timepoint: 3, 6 and 9 months after Vital Pulp Therapy. Method of measurement: Radiographic success will be determined by the absence of radiolucency in the apical or furcal region, internal or external pathologic root resorption, widening of the periodontal ligament space, and root canal calcification.

Secondary

MeasureTime frame
Patient satisfaction. Timepoint: 9 months after Vital Pulp Therapy. Method of measurement: Based on visual analog scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Nabiniya

Ilam University of Medical Sciences

fatemehnabiniya@gmail.com+98 84 3333 2864

Outcome results

None listed

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