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Root canal treatment in milk teeth using three root canal filling materials: A Double-blinded Randomized Controlled Trial.

Pulpectomies in Primary Molars Using Three Root Canal Filling Materials: A Double-blinded Randomized Controlled Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2011/06/001776
Enrollment
111
Registered
2011-06-02
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: null- 1. Non vital teeth 2. Teeth with deep carious lesion and exposures of pulp 3. Patients with the history of spontaneous pain 4. Teeth showing adequate bone support and root length

Interventions

Intervention1: pulpectomies in primary molar teeth: pulpectomies in primary molar teeth using three root canal filling materials namely RC Fill, Vitapex, and Pulpdent root canal sealer Intervention2:

Sponsors

Dr R Pramila
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Non vital teeth 2. Teeth with mild or moderate mobility [grade I and II] 3. Teeth with deep carious lesion and exposures of pulp 4. Patients with the history of spontaneous pain 5. Teeth showing adequate bone support and root length 6. Teeth with no radiographically discernable internal or pathological external resorption 7. Teeth with inter-radicular and peri-radicular radiolucencies.

Exclusion criteria

Exclusion criteria: Children with any medical history are excluded from the study.

Design outcomes

Primary

MeasureTime frame
clinical evaluation: Pain, Redness, Swelling/Abscess, Draining fistula and Mobility. Radiographic evaluation: Furcation radiolucency, Periapical radiolucency, Internal/External root resorption, Deviated eruption of succedaneous teeth, Excessive filling material and its resorption. Timepoint: Clinical and Radiographic evaluation of three root filling materials for a period of 3,6 and 12 months.

Secondary

MeasureTime frame
No Secondary Outcome measures applicable for this study.Timepoint: Not applicable

Countries

India

Contacts

Public ContactDrRPramila

Saveetha Dental College

muthumurugan@gmail.com9444045094

Outcome results

None listed

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