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Evaluating the Quality of Root Canal Fillings in Primary Molars of Children Aged 4-9 Years Using Hand and Rotary Instruments: A Randomized Clinical Trial

Evaluating the quality of obturation after pulpectomy of primary molars in children aged 4-9 years using hand and rotary instrumentation- A randomised clinical trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080459
Enrollment
62
Registered
2025-02-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: - Health Condition 2: K040- Pulpitis

Interventions

Intervention1: Kedo nano plus rotary files: To check obturation quality using Kedo nano plus rotary files for single sitting Pulpectomy procedures. Treatment will be done in 45 minute Control Interven

Sponsors

Dr Snehal Sunil Kumthekar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Children in the age group of 4-9 years 2. Children with Frankl’s behavior rating scale of definitely positive (++) and positive (+) 3. Tooth with the history of spontaneous pain 4. Tooth with irreversible pulpitis 5. Primary molars with at least remaining two third of the root length

Exclusion criteria

Exclusion criteria: 1. Children with systemic diseases and special health care needs 2. Non-vital teeth having signs of abscess, sinus and fistula 3. Primary molars with pathologic mobility and evidence of root fracture, trauma 4. Primary molars having furcation radiolucency 5. Primary molars with calcified root canals 6. Primary molars with more than two third root resorption, internal resorption and developmental anomalies 7. Patients who are not willing to undergo treatment

Design outcomes

Primary

MeasureTime frame
Obturation QualityTimepoint: Postoperative first Radiographic assessment

Secondary

MeasureTime frame
Instrumentation timeTimepoint: From starting of CMP to the last files used;Postoperative PainTimepoint: At 24hrs, 48hrs,72hrs

Countries

India

Contacts

Public ContactDr Snehal Sunil Kumthekar

KAHERs KLE V.K. Institute of Dental Sciences, Belagavi

drhugarsm@gmail.com9130418503

Outcome results

None listed

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