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A Study To Compare Different Cleaning Solutions Used During Treatment Of Infected Primary Teeth in Children

Clinical and radiographic assessment of different irrigants in enhancing the efficacy of LSTR therapy in primary molars : An in-vivo study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110402
Enrollment
60
Registered
2026-05-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: K041- Necrosis of pulp

Interventions

Intervention1: GROUP A : 0.5 % Metrogyl, GROUP B : 3 % Sodium HypoChlorite, GROUP C: 2 % Chlorhexidiene Gluconate: INTERVENTION GROUPS : 0.5 % Metrogyl, 3 % Sodium HypoChlorite, 2 % Chlorhexidiene Gl

Sponsors

HIMACHAL DENTAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children aged 3-9 years. Primary molars with signs of pulpal infection requiring LSTR treatment. Clinical signs or symptoms of pulpal infection such as: pain Tenderness on percussion, Localized swelling or abscess. Presence of spontaneous or intermittent pain characterized by sharp, dull, localized, diffuse, or referred. Presence of a sinus tract Radiographic evidence of furcation involvement, without any signs of internal or external root resorption. Teeth that were restorable and not nearing exfoliation. Children not on systemic antibiotics at the time of treatment. Children without known allergy to the antibiotics used in LSTR 3-Mix therapy (metronidazole, cefaclor and ciprofloxacin).

Exclusion criteria

Exclusion criteria: Primary molars that are grossly destructed, non-restorable, or exhibit advanced crown loss. Teeth with excessive mobility, advanced internal/external resorption, or severe furcation involvement. Children with systemic conditions contraindicating endodontic treatment. Known allergy to any of the antibiotics used in 3-Mix paste.

Design outcomes

Primary

MeasureTime frame
Assesment of different irrigants in enhancing the efficacy of LSTR therapy in primary molars using clinical and radiographic methodTimepoint: Data will be recorded at baseline followed by recall of the patient at 1, 3, 6 and 12 months for clinical and radiographic assessment. Approximately 12 months will be required per patient for completion.

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDR VINAY BAL SINGH THAKUR

Himachal Dental College And Hospital

dr.vinaythakur86@gmail.com9882855270

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026