Improving Dental Pain Relief for Kids with Molar Hypomineralization using a new device

Neuromodulation as an Adjunct to Local Anaesthesia in Paediatric Patients with MIH- A Pilot Study - nil

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/068068

Enrollment

Registered

2024-05-29

Start date

Unknown

Completion date

Unknown

Last updated

2024-06-24

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

Conditions

Health Condition 1: K004- Disturbances in tooth formation

Interventions

Intervention1: Neuromodulation using Synapse dental pain eraser, LA if required: Neuromodulation using Synapse Dental Pain Eraser will be done to acheive anesthesia in molars and Incisors affected by

Eligibility

Inclusion criteria

Inclusion criteria: ASA I or II Children aged 6-12 years. Diagnosed with Molar Incisor Hypomineralization (MIH). Requiring dental treatment under local anesthesia in either permanent molars or incisors.

Exclusion criteria

Exclusion criteria: Known neurological disorders. Allergies to local anesthetics. Contraindications to neuromodulation.

Design outcomes

Primary

Measure	Time frame
-Reduction in Pain/Hypersensitivity -Onset and Achievement of Anesthesia -Patient Acceptance -Duration of AnesthesiaTimepoint: At baseline at start of treatment at end of treatment duration of anesthesia will be measured after 30 minutes from intervention after 60 minutes form intervention	—

Secondary

Measure	Time frame
-Patient Acceptance -Duration of AnesthesiaTimepoint: immediately post treatment 30 min post treatment	—

Countries

India

Contacts

Public ContactDr Bhawna Saxena

I.T.S Dental College Hospital and Research Centre

MOUSUMI87GOSWAMI@GMAIL.COM9769892051

Outcome results

None listed

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