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The efficacy of different local anaesthetic solutions/techniques in producing painless sensation in patients suffering 'hot' mandibular tooth pulps

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN18143187
Enrollment
500
Registered
2005-11-11
Start date
2005-06-27
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

Irreversible pulpitis teeth Oral Health Dental

Interventions

The power calculation revealed that a sample size using 50 volunteer patients in each supplementary technique (four arms) will have 80% power to detect an effect size of 0.57 in a continuous outcome m

Sponsors

The Newcastle Upon Tyne Hospitals NHS Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients of 16 years of age and over 2. Any mandibular tooth with irreversible pulpitis and an asymptomatic vital tooth on the opposite site of the arch to act as an internal control of pulp tester function

Exclusion criteria

Exclusion criteria: 1. Patients with allergies or sensitivities to lidocaine/articaine or other ingredients in the anaesthetic solution 2. Patients who are unable to provide informed consent 3. Relevant medical history, which may compromise the welfare of the patient (e.g. unstable angina) or which may compromise data collection (e.g. facial paraesthesia)

Design outcomes

Primary

MeasureTime frame
To evaluate the effectiveness of initial IANB in profoundly anaesthetising irreversibly pulpitic and adjacent non-pulpitic.

Secondary

MeasureTime frame
To evaluate the effect of supplementary local anaesthetic techniques after failure of pulp anaesthesia by IANB in patients suffering mandibular irreversible pulpitis.

Countries

United Kingdom

Outcome results

None listed

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