The clinical research evaluating intradermal administration with the intradermal injection system

The clinical research evaluating intradermal administration with the intradermal injection system - The clinical research evaluating intradermal administration with the intradermal injection system

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000010777

Enrollment

Registered

2013-08-01

Start date

2014-02-18

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 individuals patients taking steroid

Interventions

saline by intradermal injection saline by subcutaneous injection

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: -A person 20 years of age or older -Those whom written informed consent is obtained from -Healthy person -A person with skin disease -A person who takes steroid

Exclusion criteria

Exclusion criteria: -A person who has any abnormality in the application site. -A person who are deemed to have experience or high risk of hypersensitivity for drugs used in this study. -A person who are deemed to have high risk to ultra-sound imaging examination. -Those who have experience gave rise to skin conditions such as contact dermatitis due to materials of the products (such as stainless steel and silicone oil) used in this study. -Those who are deemed inappropriate to participate in this study by doctor.

Design outcomes

Primary

Measure	Time frame
Skin property Injection site examination Injection Pain Skin image examination	—

Countries

Japan

Contacts

Public ContactHideaki Tanizaki

Kyoto University Hospital Department of Dermatology

tanizaki@kuhp.kyoto-u.ac.jp075-751-3111

Outcome results

None listed

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