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Efficacy of Tiotropium bromide (Spiriva 2.5 microgram Respimat 60 puffs) for chronic asthmatic cough refractory to intensive therapies

Efficacy of Tiotropium bromide (Spiriva 2.5 microgram Respimat 60 puffs) for chronic asthmatic cough refractory to intensive therapies - Efficacy of Tiotropium bromide (Spiriva 2.5 microgram Respimat 60 puffs) for chronic asthmatic cough refractory to intensive therapies

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000021064
Enrollment
60
Registered
2016-02-24
Start date
2016-02-26
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

asthma

Interventions

Add on tiotropium bromide(5 microgram/day). Add on theophylline (400 mg/day).

Sponsors

Nagoya City University Dept of Respiratory Medicine, Allergy and Clinical Immunology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with chronic asthmatic cough lasting for 8 weeks or more despite adequate treatments including inhaled corticosteroids and long-acting adrenergic bronchodilator

Exclusion criteria

Exclusion criteria: If patients meet the following criteria, they are excluded. Patients who have other respiratory disease such as tuberculosis or lung cancer. currently smoke, had smoking history with 10 pack-years or more, or had quitted smoking within 6 months prior to the enrollment. have already taken anti-cholinergic agents or xanthin. have already taken some medicines with anti-cholinergic effects have allergy for anti-cholinergic agents or xanthin. have benign prostatic hypertrophy with dysuria. have closed-angle glaucoma. are during pregnancy or lactaion, or have possibility of pregnancy.

Design outcomes

Primary

MeasureTime frame
To evaluate the changes of the degree of cough severity and the cough-specific quality of life before and 4 weeks after the treatment intervention, with a use of Cough Visual Analogue Scale and Leicester Cough Questionnaire, respectively

Secondary

MeasureTime frame
To evaluate the changes of capsaicin cough reflex sensitivity and several biomarkers before and 4 weeks after the treatment intervention

Countries

Japan

Contacts

Public ContactKensuke Fukumitsu

Nagoya City University Dept of Respiratory Medicine, Allergy and Clinical Immunology

k-fkmt@med.nagoya-cu.ac.jp052-853-8216

Outcome results

None listed

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