Painless Anesthesia for mandibular teeth

A comparative efficacy of a new anesthetic technique with conventional nerve block Anesthesia - A randomised double blinded clinical trial - A pilot study

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2016/12/007546

Enrollment

656

Registered

2016-12-07

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- patients with irreversible pulpitis

Interventions

Intervention1: CAT - Customised anesthetic technique: Based on ex vivo study, new technique developed for south indian population for mandibular anaesthesia Control Intervention1: Conventional Inferio

Eligibility

Inclusion criteria

Inclusion criteria: irreversible pulpitis. Patient with moderate to severe spontaneous pain and exhibited a positive response to the electric pulp test (EPT).Only patients with moderate to severe pain were taken up for this study (NRS > 4).

Exclusion criteria

Exclusion criteria: Exclusion criteria included any reported allergy to local anesthetic agents, unstable cardiovascular disease and pregnancy, neurologic disorders with sensory disturbance and not able to provide written

Design outcomes

Primary

Measure	Time frame
anesthetic successTimepoint: 31.12.16	—

Secondary

Measure	Time frame
Pain of needle insertionTimepoint: 15minutes from time of injection	—

Countries

India

Contacts

Public ContactJames D Raj

saveetha dental college

drsinramesh@gmail.com9840136543

Outcome results

None listed

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