Skip to content

[Study of Tulobuterol Patch] Diagnostic procedure for infantile bronchial asthma <Pilot Study> -Evaluation of Tulobuterol Patch using pulse oximetry-

[Study of Tulobuterol Patch] Diagnostic procedure for infantile bronchial asthma <Pilot Study> -Evaluation of Tulobuterol Patch using pulse oximetry- - [Study of Tulobuterol Patch] Diagnostic procedure for infantile bronchial asthma <Pilot Study> -Evaluation of Tulobuterol Patch using pulse oximetry-

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009904
Enrollment
30
Registered
2013-01-30
Start date
2012-11-02
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

infantile bronchial asthma

Interventions

Hokunalin tape 0.5 mg is applied on chest, back, or upper arm at 8 pm once daily.

Sponsors

Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: i.Patients who present with respiratory symptom and have suspected bronchial asthma. ii.Patients who have not had a major attack of bronchial asthma during one week prior to initiation of study drug.

Exclusion criteria

Exclusion criteria: i.Patients receiving an inhaled long-acting beta-2 agonist (inhaled salmeterol) or receiving an oral short-acting beta-2 agonist continuously. ii.Patients who have known hypersensitivity to Tulobuterol Patch or have a skin disease, including atopic dermatitis, and are considered inappropriate to use Tulobuterol Patch. iii.Patients who have thyroid hyperfunction disorders, hypertension, cardiac disorder, or diabetes concurrently, and are considered inappropriate to use a beta-2 antagonist. iv.Patients who have experienced serious adverse drug reactions of Tulobuterol. v.Patients who, in the opinion of the investigator are inappropriate for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
SpO2 that will be measured using pulse oximetry for at least three hours around 4 am while the patient is sleeping

Countries

Japan

Contacts

Public ContactTakahide Teramoto

Graduate School of Medicine Pediatrics

058-230-6386

Outcome results

None listed

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