Skip to content

Comparison of adherence and efficacy between inhaled salmeterol and transdermal tulobuterol patch in elderly COPD patients

Comparison of adherence and efficacy between inhaled salmeterol and transdermal tulobuterol patch in elderly COPD patients - Comparison of adherence and efficacy between inhaled salmeterol and transdermal tulobuterol patch

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001503
Enrollment
26
Registered
2008-11-13
Start date
2006-09-01
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

COPD

Interventions

We conducted a randomized, crossover study comparing the adherence to and efficacy of LABA between the transdermal tulobuterol patch (TP, 2 mg once a day) and inhaled salmeterol (50 &amp
g, twice a day) in elderly COPD patients. We conducted a randomized, crossover study comparing the adherence to and efficacy of LABA between the transdermal tulobuterol patch (TP, 2 mg once a day) an
g, twice a day) in elderly COPD patients.

Sponsors

The Tokyo Metropolitan Geriatric Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients had clinical features consistent with the presence of moderate-to-severe COPD including the spirometric criteria of post-bronchodilator FEV1/FVC ratio of less than 0.7 and FEV1 between 30% and 80% of the predicted values for height and age, and their condition remained stable during the past month.

Exclusion criteria

Exclusion criteria: The exclusion criteria included age younger than 65 years, dementia and any previously use of inhaled medications such as 2-agonists, anti-cholinergics or corticosteroids, patched 2-agonist, or systemic corticosteroids. Patients with dermatological disorders, severe heart diseases, uncontrolled hypertension or other diseases for which patch preparations or treatments with 2-agonists was considered inappropriate were also excluded.

Design outcomes

Primary

MeasureTime frame
The primary outcomes were adherence to the medication and change in a 6-minute walk distance (6MWD).

Secondary

MeasureTime frame
The secondary outcomes were spirometric values and quality of life (QOL) measured by the St.George's Respiratory Questionnaire.

Countries

Japan

Contacts

Public ContactHideki Takahashi

The Tokyo Metropolitan Geriatric Hospital Division of Respiratory Medicine

03-3964-1141t

Outcome results

None listed

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