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Montelukast Sodium Tablets treatment clinical study for intractable cough by idiopathic pulmonary fibrosis

Montelukast Sodium Tablets treatment clinical study for intractable cough by idiopathic pulmonary fibrosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-15005841
Enrollment
Unknown
Registered
2015-01-17
Start date
2015-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Idiopathic pulmonary fibrosis

Interventions

Montelukast Sodium Tablets treatment group :Montelukast Sodium Tablets: oral, 1 tablets each time (10mg), 1 time a day, at bedtime, for a period of 12 weeks
control group :Don't take Montelukast Sodium Tablets

Sponsors

Shanghai Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Idiopathic pulmonary fibrosis (IPF) patients are diagnosed according to the 2011 ATS / ERS /JRS / ALAT criterion; 2. patients with intractable cough, cough scores equal to or greater than 2; 3. Male or female; aged during 50 to 80 years old; 4. Have good compliance, willing to exercise in accordance with the program and follow-up with the schedule; 5. Patients were fully informed of the purpose, method and possible discomfort of the test, agree and signed in consent.

Exclusion criteria

Exclusion criteria: 1. With lung infections need antibiotic treatment; 2. patients with asthma; 3. patients with malignant tumor; 4. patients with serious diseases in other system and organ dysfunction; 5. Pregnancy, breast-feeding women, planning to pregnant and those who can not take effective contraceptive measures; 6. patients with obvious abnormal liver or kidney function, ALT or AST value greater than 1.5 times of normal; Cr value greater than 1.5 times of normal; 7. allergic to Montelukast Sodium Tablets; 8. Participating in other clinical trials within three months; 9. People who can't express discomfort; 10. There is any unsuitable situation for those selected.

Design outcomes

Primary

MeasureTime frame
cough score;Visual analogue scale;Efficiency evaluation;

Contacts

Public ContactHuiping Li
liw2013@126.com+86 13817389991

Outcome results

None listed

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