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Comparison of gel formulation of Silver diamine fluoride ( a caries arresting agent ) with conventional solution to stop caries in primary teeth .

Comparative evaluation of caries arrest potential of silver diamine fluoride gel with conventional solution form in primary teeth- A randomized controlled trial. - nil

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/079990
Enrollment
252
Registered
2025-02-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: K029- Dental caries, unspecified

Interventions

Intervention1: 38% Silver diamine Fluoride gel with potassium iodide: it is a caries preventive agent with a gel forming agent that is applied on to carious tooth under cotton pellets isolation to arr

Sponsors

Dr. Ligam Padu
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1-Healthy children from the age of 4-8 years 2-Child having at-least one asymptomatic active cavitated lesion in primary tooth 3-Children whose cooperation level is scored as positive or definitely positive as per Frankl Behaviour Rating Scale

Exclusion criteria

Exclusion criteria: 1-Teeth with pain, or any other symptoms suggestive of pulpitis 2-Teeth with signs of irreversible of irreversible pulpitis (spontaneous pain, abscess, pathological mobility) 3-Teeth suggesting signs of non-vital pulp. 4-Children having significant chronic systematic condition or taking long term medication that may affect oral health 5-Children whose parents don t give consent for the SDF application 6-Children with known allergy to silver

Design outcomes

Primary

MeasureTime frame
To compare and evaluate the caries arrest potential of novel Silver Diamine Fluoride gel and Conventional SDF solution in cavitated carious lesions in primary teethTimepoint: Baseline, 1 month, 6 month, 12 month

Secondary

MeasureTime frame
1-To compare the taste acceptability of the patient 2-Parental acceptance levelTimepoint: Taste acceptability will be assessed at the baseline at the time of application of the SDF sol or gel. Parent acceptance level will be assessed at 6 month follow up visit

Countries

India

Contacts

Public ContactDr Ligam Padu

All India Institute of Medical Sciences

drkalpanabansal@gmail.com9810105132

Outcome results

None listed

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