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Comparison of Miniature Pulpotomy with Full Pulpotomy

To Compare Miniature Pulpotomy v/s Full Pulpotomy in Carious Non-Exposed Molars -An In-Vivo Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046451
Enrollment
72
Registered
2022-10-13
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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: Pulpotomy: Full Pulpotomy in Carious Non Exposed Molars in 48 hours, 60 hours, 7 days, 3 months, 6months Control Intervention1: Pulpotomy: Miniature Pulpotomy In Carious Non Exposed Mol

Sponsors

Neha Chawda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient aged 14-60 years Permanent molar teeth with closed apex Symptoms- range from mild to non- spontaneous pain Positive response to pulp sensibility test Presence of moderately deep carious lesions on radiograph Pulp exposure after non selective caries removal

Exclusion criteria

Exclusion criteria: Patient aged less than 14 years and more than 60 years Patients on analgesics , blood thinners Incisors or canines or premolars heavily restored or non restorable teeth presence of deep and extremely deep carious lesions on radiograph Patient has moderate-severe pain Negative response to pulp sensibility test Pulp not exposed intra-operatively Presence of ââ?¬Å?soundââ?¬? dentine over pulp Pulp necrosis evident on after caries removal Pulpal haemorrhage could not be arrested Pregnant women

Design outcomes

Primary

MeasureTime frame
To compare performance of miniature pulpotomy and full pulpotomy in mild and moderate pulpitis in posterior teeth using a biodentine materialTimepoint: 48 hours 60 hours 7 days 3 months 6 months

Secondary

MeasureTime frame
To compare pain (Vas scale) between two groups To compare for the clinical success rate between two groups To compare the radiographic outcomes between two groups (using paralleling cone technique) To compare the overall success rate between two groups Timepoint: 48 hours 60 hours 7 days 3 months 6 months

Countries

India

Contacts

Public ContactDr Sonali Kapoor

Manubhai Patel Dental College and Hospital and ORI

drsonalikapoor@mpdentalcollege.edu.in9825323057

Outcome results

None listed

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