Skip to content

Wand STA vs SleeperOne for Pediatric Local Anesthesia (WASO-Kids)

A Randomized Controlled Trial of the Acceptance of Two Computer-controlled Anaesthetic Delivery Systems in Paediatric Patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07754851
Acronym
WASO-Kids
Enrollment
72
Registered
2026-08-10
Start date
2025-05-05
Completion date
2026-01-30
Last updated
2026-08-10

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

Conditions

Dental Anxiety, Pain Management

Keywords

wand sta, sleeper one, compute red-controlled anesthetic delivery, cclad, pediatric dentistry, local anesthesia, dental injection, child behavior

Brief summary

This randomized, single-blind, split-mouth trial compares the acceptance of two computer-controlled local anaesthetic delivery (CCLAD) systems - Wand® STA and SleeperOne⑤ - in children aged 4-9 years undergoing comparable bilateral dental treatment. Each child receives local anaesthesia via both devices at separate visits, with pain, behaviour, heart rate, and oxygen saturation recorded at each session, to determine whether the two systems differ in child acceptance and physiological response.

Interventions

DEVICEComputer-controlled local anesthetic delivery system (pressure-sensing, single-tooth anesthesia type)

A computer-controlled device that delivers local anesthetic through a pen-like handpiece at a constant, programmable flow rate and pressure. Incorporates pressure sensing to enable single-tooth anesthesia via periodontal ligament or infiltration delivery with minimal soft-tissue numbness. Articaine 1:200,000 was administered via this system at one of the two study visits, according to randomized sequence assignment.

DEVICEComputer-controlled local anesthetic delivery system (corded, pen-style electronic type)

A corded, pen-style computer-controlled device that delivers local anesthetic at a programmable injection speed across conventional, intraligamentary, and, in suitable cases, intraosseous techniques. Articaine 1:200,000 was administered via this system at one of the two study visits, according to randomized sequence assignment.

Sponsors

National and Kapodistrian University of Athens
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Intervention model description

Crossover Assignment (split-mouth design; each participant serves as their own control)

Eligibility

Sex/Gender
ALL
Age
4 Years to 9 Years
Healthy volunteers
Yes

Inclusion criteria

* Non-contributory medical history * At least one tooth requiring the same treatment on each side of the same jaw * Teeth on both sides with normal periodontium and no periapical pathology (confirmed radiographically)

Exclusion criteria

* Age outside 4-9 years * History of psychiatric or developmental illness, or allergies * Use of analgesic medication in the preceding 12 hours * History of unpleasant dental treatment experiences

Design outcomes

Primary

MeasureTime frameDescription
Assessed at the end of each anaesthesia session, at both the first and second study visitsPeriproceduralAfter the second anaesthetic injection, children rated their pain or discomfort using the Wong-Baker FACES Pain Rating Scale, administered by a trained examiner blinded to which device had been used. The scale presents six faces corresponding to scores of 0, 2, 4, 6, 8, and 10, where 0 indicates "no hurt" and 10 indicates "hurts worst"; higher scores indicate greater pain (a worse outcome). Children selected the face that best matched how they felt immediately after the injection
Wong-Baker FACES Pain Score During Local Anaesthesia InjectionImmediately following completion of the first local anaesthesia injection, prior to the start of dental treatmentAfter each anaesthetic injection, children rated their pain or discomfort using the Wong-Baker FACES Pain Rating Scale, administered by a trained examiner blinded to which device had been used. The scale presents six faces ranging from 0 (no hurt) to 10 (hurts worst), with children selecting the face that best matched how they felt. Scores were recorded once per session, after the first (Wand® STA or SleeperOne⑤, per randomized sequence) and again after the second anaesthetic delivery visit, allowing comparison both between devices and between sessions.

Countries

Greece

Contacts

PRINCIPAL_INVESTIGATORKatechi

NKUA

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 11, 2026