A single-institutional study for the efficacy and optimal dose and method of Japanese herbal medicine in pediatric patients

A single-institutional study for the efficacy and optimal dose and method of Japanese herbal medicine in pediatric patients - A single-institutional study of Japanese herbal medicine in pediatric patients

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000023090

Enrollment

700

Registered

2016-07-11

Start date

2016-07-11

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

Pediatric diseases

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. All patients with pediatric surgical disease, visiting our outpatient clinic or hospitalized in our institute. 2. All patients are required to give written informed consent prior to enrolment in the study. 3. Patients who are under 10 years old are required to give written informed consent from proxy. 4. Patients who are aged over 10 years and below 20 years are required to give written informed assent and written informed consent from proxy.

Exclusion criteria

Exclusion criteria: 1. Known allergy or contraindication to Japanese herbal medicine 2.Patients whom investigators consider to be ineligible

Design outcomes

Primary

Measure	Time frame
Efficacy	—

Secondary

Measure	Time frame
Safety, medication adherence, optimal method, consciousness, and survey	—

Countries

Japan

Contacts

Public ContactKohei Otake

Mie University Graduate School of Medicine Department of Gastrointestinal and Pediatric Surgery

kohei815@clin.medic.mie-u.ac.jp059-232-1111(5645)

Outcome results