Skip to content

A clinical trial to evaluate the treatment outcome of two medications used as root canal filling materials in children with primary tooth infections.

Evaluation of treatment outcome in terms of clinical and radiographic presentation of Chitra HAP-fil TM and Zinc oxide Eugenol as pulpectomy medicaments in primary mandibular molars- A Randomised controlled trial. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073303
Enrollment
60
Registered
2024-09-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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: Chitra HAP-Fil TM: Each tooth will be anesthetized and isolated with a rubber dam. Following the access opening using sterile round carbide burs, the working length (WL) will be determi

Sponsors

Dr Sruthi Priyadharshiny S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children with signs of irreversible pulpitis in primary mandibular molars. Teeth should have adequate bone support with at least 2/3rd of intact root length with neither gingival swelling nor sinus tract.

Exclusion criteria

Exclusion criteria: Grossly decayed teeth which cannot be restored. Any pathologic signs of external or internal resorption of the roots. Children with underlying systemic diseases and with special health care needs and those who exhibit negative and definitely negative Frankl behavior rating.

Design outcomes

Primary

MeasureTime frame
Radiographic Success assessed by RVG (Absence of: Furcation radiolucency, Abnormal root resorption, Deviated eruption of succedaneous teeth, Excess filling material and its resorption)Timepoint: 9 months post-intervention period.

Secondary

MeasureTime frame
Clinical success (Absence of Pain, Swelling, Fistulous opening, & Abnormal mobility)Timepoint: 9 month post-intervention period;Quality of Obturation assessed with RVG using Coll & Sadrian criteria, 1996.Timepoint: Immediate post-intervention period

Countries

India

Contacts

Public ContactDr Jeeva PP

Government Dental College, Kottayam

jeevareghu@gmail.com9447300050

Outcome results

None listed

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