Comparative evaluation of Anesthetic Efficacy of needleless anesthesia and conventional anesthesia in patients with Symptomatic irreversible pulpitis. A Randomized Clinical Trial

Comparative Evaluation of Anesthetic Efficacy of needleless anesthesia and conventional anesthesia in patients with Symptomatic irreversible pulpitis. A Randomized Clinical Trial

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/12/038471

Enrollment

Registered

2021-12-07

Start date

Unknown

Completion date

Unknown

Last updated

2022-02-21

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

Conditions

Health Condition 1: K040- Pulpitis

Interventions

Intervention1: Needleless anesthesia: Comfort-in (Needle Free Injection System) Control Intervention1: Conventional Local anesthesia: Giving Local Anesthesia with syringes

Eligibility

Inclusion criteria

Inclusion criteria: Pa1ents with symptoma1c irreversible pulpi1s

Exclusion criteria

Exclusion criteria: periapical lesion, individuals allergic to local anesthesia, pregnant woman,alcoholics,drug users.

Design outcomes

Primary

Measure	Time frame
Onset, depth of anaesthesiaTimepoint: 15 minutes from time of injection	—

Secondary

Measure	Time frame
NilTimepoint: Nil	—

Countries

India

Contacts

Public ContactDr Iffat Nasim

Saveetha Dental College & Hospital

nasimiffat@gmail.com9940063567

Outcome results

None listed

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