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Effect of the new surface anesthesia at the time of injection

Effect of the new surface anesthesia at the time of injection - Effect of the new surface anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000030402
Enrollment
20
Registered
2018-01-04
Start date
2018-01-04
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

None

Interventions

Usage of the new surface anesthesia

Sponsors

Yamaguchi University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patient who will receive blood draw or infusion more than twice during observation period.

Exclusion criteria

Exclusion criteria: The patient who have allergy against lidocaine, aminobenzoate or adrenalin. The patient who have possibility of pregnancy or nursing.

Design outcomes

Primary

MeasureTime frame
The reduced level of the pain of needle at the time of injection by the new surface anesthesia

Countries

Japan

Contacts

Public ContactHarada Koji

Yamaguchi University Graduate School of Medicine Department of Oral and Maxillofacial Surgery

harako@yamaguchi-u.ac.jp0836-22-2299

Outcome results

None listed

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