Evaluation of pharmacokinetics of bisoprolol after apprication of a bisoprolol patch preparation for an 8 h.

Evaluation of pharmacokinetics of bisoprolol after apprication of a bisoprolol patch preparation for an 8 h. - Evaluation of pharmacokinetics of bisoprolol after apprication of a bisoprolol patch preparation for an 8 h.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000023024

Enrollment

Registered

2016-07-15

Start date

2016-07-15

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 adult

Interventions

Application of a patch preparation containing 4 mg bisoprolol for 8 h

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: 1. Healthy male Japanese. 2. Volunteers being able to make self-judgment to participate in this study and giving written informed consent. 3. Volunteers judged to be appropriate for this study by chief doctor.

Exclusion criteria

Exclusion criteria: 1. Having disease to be cured now. 2. Having drug/cutaneous allergy or its past history. 3. Volunteers rejected participating in this study by chief doctor.

Design outcomes

Primary

Measure	Time frame
Pharmacokinetic parameter	—

Secondary

Measure	Time frame
Release from preparation	—

Countries

Japan

Contacts

Public ContactKazuyuki Ueno

Niigata University of Pharmacy and Applied Life Sciences Department of Clinical Pharmacokinetics, Faculty of Pharmaceutical Sciences

uenok@nupals.ac.jp0250-25-5278

Outcome results

None listed

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