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Effects of tiotropium bromide and odardarol maleate on perioperative lung function and small airway function in patients with lung cancer complicated with severe/very severe COPD

Effects of tiotropium bromide and odardarol maleate on perioperative lung function and small airway function in patients with lung cancer complicated with severe/very severe COPD

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022649
Enrollment
Unknown
Registered
2019-04-20
Start date
2019-04-30
Completion date
Unknown
Last updated
2019-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COPD

Interventions

Double-drug trial group:Tiotropium bromide odardarol and indardarol maleate were used since admission
Single drug group:Tiotropium bromide was used since admission

Sponsors

Shanghai Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: (1) aged 18-79 years; (2) in accordance with the Chinese medical association respiratory neurology, chronic obstructive pulmonary disease committee for the guidance of diagnosis and treatment of chronic obstructive pulmonary disease (2013 revision) "set of diagnostic criteria, group C or D in lung function class for III - IV namely; (3) receive inhalation therapy; (4) informed consent, and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) allergy to tiotropium bromide and odardarol/indardarol maleate or any inhaled components of inhalants; (2) patients with bronchial lung cancer, dilatation, interstitial lung disease or other diseases are not suitable for inhalation therapy; (3) other systemic diseases, including heart, liver, kidney, hematopoietic, nervous system diseases, glaucoma, severe prostatic hyperplasia; (4) doctors consider it inappropriate to take bronchodilators; (5) intraoperative lobectomy changes; (6) cannot tolerate one-lung ventilation; (7) when the woman is pregnant or breast-fed; (8) the patient is accompanied by other malignant tumors; (9) anticholinergic drugs were used in the first 4 weeks of the study, and has a history of acute episodes or antibiotics were used; has received systemic glucocorticoid therapy in the past two months; (10) With heart, liver, kidney or endocrine diseases.

Design outcomes

Primary

MeasureTime frame
FEV1;FEV1%;MMEF;

Countries

China

Contacts

Public ContactChang Chen

Shanghai Pulmonary Hospital

chenthoracic@163.com+86 13816839003

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026