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Efficacy of incisive nerve block for pulp anaesthesia in the mandible

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN53304116
Enrollment
38
Registered
2008-05-09
Start date
2008-05-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Anaesthesia in the mandible Oral Health N/A

Interventions

This is a randomised, double-blind, cross-over study. Each volunteer will receive 2 incisive nerve block injections in the mouth, one with and one without massage of the injection site, in random orde

Sponsors

Newcastle upon Tyne Hospitals NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy adult volunteers 2. Staff or students at the Newcastle University

Exclusion criteria

Exclusion criteria: The volunteers: 1. Individuals under 18 years old 2. Systemic disorders which may place volunteers at risk from local anaesthetic injection for example bleeding disorder, history of infective endocarditis, pregnant women 3. Allergies to local anaesthetics 4. Facial anaesthesia or paraesthesia 5. In dental pain at the time of trial 6. Individuals unable to give informed consent form The teeth: 1. Teeth which respond negatively to baseline pulp testing 2. Key test teeth missing

Design outcomes

Primary

MeasureTime frame
Numbness of lower teeth (back teeth) following local anaesthetic injection. This will be assessed by electric pulp testing every 2 minutes after injection for the first 10 minutes then every 5 minutes until 45 minutes.

Secondary

MeasureTime frame
1. Injection discomfort, assessed with a visual analogue scale at each visit 2. Duration of numbness after injection

Countries

United Kingdom

Outcome results

None listed

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