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clinical and radiographic success rate of three different pulp therapy materials in milk teeth

A Comparative Evaluation of Bioactive Glass and 3Mixtatin with Mineral Trioxide Aggregate as Pulpotomy Medicaments in Primary teeth: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/032336
Enrollment
72
Registered
2021-03-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K040- Pulpitis

Interventions

Intervention1: 3Mixtatin: A newer emerging material in regenerative dentistry is 3mixtatin combination of 3Mix antibiotic paste (100mg metronidazole, 100mg ciprofloxacin, 100mg cefixime) and 2mg simva

Sponsors

Dr Gunna Madhuri
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pediatric patients between the age groups of 3 to 9 years irrespective of gender. Primary molars with carious exposures of pulp. Primary molars without any signs of pulpal degeneration Primary molars with intracanal hemorrhage of bright red in color and successful hemorrhage control within 5 min of the removal of the coronal pulp. Radiographic evidence of at least two-thirds of the root length

Exclusion criteria

Exclusion criteria: Primary teeth having previous or attempted pulpotomy, pulpectomy or root canal treatment Primary teeth showing signs or symptoms of pulpal necrosis, spontaneous pain, history of swelling or abscess or �stula or sinus tract, pain at night, pathologic mobility, and tenderness on percussion. Primary teeth that need greater than 5 minutes to achieve haemostasis. Primary teeth when �nal restoration with stainless steel crown is not possible. Radiographic evidence of internal or external pathologic root resorption, periapical or furcal radiolucency, and more than one-third of root resorption. Primary teeth without a permanent successor.

Design outcomes

Primary

MeasureTime frame
Clinically: For Pain, Swelling, Sinus tract formation, Gingival Swelling, Tooth mobility. Radiographically: Periodontal ligament changes, Periapical changes, Internal and External tooth resorption, Normal or Abnormal Exfoliation of the toothTimepoint: 3, 6, 9, and 12 months—

Secondary

MeasureTime frame
Cost factor, Manipulation time and handling of materials used as pulpotomy materialsTimepoint: 1,3 months—

Countries

India

Contacts

Public ContactDr Afroz Alam Ansari

Faculty of Dental Sciences, King Georges Medical University

madhurileo26@gmail.com9642895699

Outcome results

None listed

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