Skip to content

EVALUATION OF PAIN AFTER SINGLE SITTING ROOT CANAL TREATMENT USING HAND AND ROTARY INSTRUMENTS

COMPARATIVE EVALUATION OF POST-OPERATIVE PAIN AFTER SINGLE SITTING PULPECTOMY USING HAND AND ROTARY INSTRUMENTATION IN PRIMARY MOLARS OF CHILDREN â?? A RANDOMISED CONTROL STUDY - PAHRI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/12/029470
Enrollment
60
Registered
2020-12-01
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: Pediatric rotary files: The operator (Principal Investigator) shall perform all the procedures under Standard Operating Protocols. Local anesthesia will be given and rubber dam will be

Sponsors

Department of Pediatric and Preventive Dentistry
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Children in the age group of 4-8 years. 2. Children with Franklâ??s behaviour rating scale of positive (+) and definitely positive (++). 3. Tooth with the history of spontaneous pain. 4. Radiographic evaluation of the tooth showing irreversible pulpitis. 5. Primary molars with minimum two third of the root length. 6. Patients who are willing to undergo treatment

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
Post operative painTimepoint: 24 hours 48 hours 72 hours

Secondary

MeasureTime frame
Reduction in pain, swelling and increasing the quality of lifeTimepoint: After 24hours, 48 hours, 72hours

Countries

India

Contacts

Public ContactDr Nivedita Saxena

KLE VK Institute of Dental Sciences.

dr.hugarsm@gmail.com9986436448

Outcome results

None listed

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