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Acceptability of the Wand® local anaesthetic device for young dental patients

Assessing the acceptability of the Wand® computer-controlled local anaesthetic device for paediatric dental patients: A pilot clinical trial

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN48966094
Enrollment
30
Registered
2021-03-10
Start date
2021-07-01
Completion date
Unknown
Last updated
2021-08-02

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

Conditions

Assessing Wand® local anaesthetic acceptance in young dental patients Oral Health

Interventions

Trial procedure: 1- Pre-intervention assessments Patients will be screened for eligibility against the inclusion criteria for their age (10-16 yrs), their medical histo

Sponsors

Libyan Ministry of Education
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Paediatric patients aged 10 - 16 years 2. No previous experience of having LA delivered by the Wand® 3. Requiring dental treatment under LA 4. Good general health (American Society of Anaesthesiology ASA classification I & II) 5. Able to understand English sufficiently to complete scales/rating profiles appropriately 6. Patients and guardians willing to give informed assent/consent to participate in the study 7. Co-operative, with no indication of conscious sedation or treatment under general anaesthesia

Exclusion criteria

Exclusion criteria: 1. Aged below 10 or over 16 years old 2. Children unable to understand English sufficiently 3. Requiring treatment under conscious sedation or general anaesthesia 4. Children with ASA class III or over 5. Patients who have previously received dental anaesthesia using the Wand® 6. Unwilling to give consent

Design outcomes

Primary

MeasureTime frame
Measured before and after dental treatment during the single visit: 1. Acceptability of local anaesthetic received using a VAS 2. Level of anxiety before using a novel questionnaire

Secondary

MeasureTime frame
There are no secondary outcome measures

Countries

United Kingdom

Outcome results

None listed

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