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Comparison of topical anesthetics to relieve venipuncture pain: a randomized controlled trial.

Comparison of topical anesthetics to relieve venipuncture pain: a randomized controlled trial. - Comparison of topical anesthetics to relieve venipuncture pain: a randomized controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011463
Enrollment
24
Registered
2013-08-12
Start date
2013-08-13
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Healthy adults Healthy children

Interventions

1. lidocaine-prilocaine cream (Right Arm) 2. high-dose lidocaine cream (Left Arm) 1. high-dose lidocaine cream (Left Arm) 2. lidocaine-prilocaine cream (Right Arm) 1. high-dose lidocaine cream (Righ

Sponsors

National Center for Child Health and Development
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Staff of National Center for Child Health and Development 2) Volunteers who are provided informed, written consent for participation in Japanese

Exclusion criteria

Exclusion criteria: 1. Volunteers who have hypersensitivity to anesthetic agents 2. Volunteers who have skin diseases (erosion or eczema) on the upper arms and/or hands 3. Volunteers who have a experience of blood exam using lidocaine-prilocaine cream or high-dose lidocaine cream 4. Volunteers who judges that the physician is inappropriate

Design outcomes

Primary

MeasureTime frame
Score of visual analog scale

Secondary

MeasureTime frame
1. Duration time for blood sampling 2. Site of blood sampling 3. Persons who take blood samples 4. Dose of blood samples 5. Times of venipuncture 6. Side effects

Countries

Japan

Contacts

Public ContactNobuaki Michihata

National Center for Child Health and Development Department of Postgraduate Education and Training

michihata-tky@umin.org03-3416-0181

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026