The effect of Yokukansan suppository to prevent emergence agitation after general anesthesia in pediatric patients

The effect of Yokukansan suppository to prevent emergence agitation after general anesthesia in pediatric patients - The effect of Yokukansan suppository to prevent emergence agitation after general anesthesia in pediatric patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000026687

Enrollment

100

Registered

2017-03-28

Start date

2017-03-28

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

The pediatric patients undergoing strabismus surgery or tonsillectomy

Interventions

pateients are received Yokukansan suppository 0.2g/kg at induction of anesthesia pateients are received only suppository base at induction of anesthesia

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists physical status 1 or 2 and scheduled to undergo strabismus surgery or tonsillectomy under general anesthesia.

Exclusion criteria

Exclusion criteria: Patients who have the medial history such as mental retardation, mental disease, taking psycotropics.

Design outcomes

Primary

Measure	Time frame
The emergence agitation in PACU(PAED scale>10)	—

Countries

Japan

Contacts

Public ContactKa Koui

Kanagawa children's medical centre Department of Anesthesiology

kka@kcmc.jp045-711-2351

Outcome results

None listed

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