To evaluate the effect of Low Level lasers, external vibrating device & lignocaine gel for pain reduction during intra oral injections

Comparative evaluation of effectiveness of External vibrating device and Low Level Laser therapy on pain perception during local anaesthetic administration. - nil

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061382

Enrollment

Registered

2024-01-11

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-01

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: Low level Laser therapy: applied in the buccal vestibule of maxilla or mandibule on right side arch for 30 secs, prior to intraoral injection with a frequency of 810nm power 1.5watt Int

Eligibility

Inclusion criteria

Inclusion criteria: Children with good general health Frankel Behaviour rating of 3 and 4 requiring administration of local anesthesia willing to participate with parents consent are included

Exclusion criteria

Exclusion criteria: Medically compromised children, children with active pathosis in the injection region and any history of allergy to Local Anaesthesia are excluded from the study

Design outcomes

Primary

Measure	Time frame
To compare & evaluate the pain perception following topical application of Low Level Lasers, buzzy bee device & commercially lidocaine gelsTimepoint: 30 secs after application	—

Secondary

Measure	Time frame
to evaluate any adverse effects following their applicationTimepoint: 10mins after application	—

Countries

India

Contacts

Public ContactDR SHRUTHA S P

AMES Dental college and Hospital

raghavendrahavale@yahoo.co.in9448407300

Outcome results

None listed

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