study of the efficacy of the Levobupivacaine in mandibular-foramen conduction anesthesia

study of the efficacy of the Levobupivacaine in mandibular-foramen conduction anesthesia - study of an analgesic effect and duration of action

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000009341

Enrollment

Registered

2012-11-30

Start date

2012-12-01

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

adult

Interventions

Mandibular-foramen conduction anesthesia is performed by 2.0mL of 0.25%Levobupivacaine hydrochloride Mandibular-foramen conduction anesthesia is performed by 2.0mL of 2%Lidocaine hydrochloride with 1/

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: the adult fully explained about this study and consent was got

Exclusion criteria

Exclusion criteria: the adult fully explained about this study and consent was not got

Design outcomes

Primary

Measure	Time frame
1.anesthesia success rate 2.onset of anesthesia time 3.pulp chamber anesthesia success rate 4.unpleasant frequency at the time of infusion of drug	—

Countries

Japan

Outcome results

None listed

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