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Effect of JINSHIHOUTOU for patients with Pulmonary Mycobacterium avian complex infection

Effect of JINSHIHOUTOU for patients with Pulmonary Mycobacterium avian complex infection - Effect of JINSHIHOUTOU for MAC patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000033590
Enrollment
30
Registered
2018-08-01
Start date
2018-03-01
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

pulmonary Mycobacterium avian complex infection

Interventions

JINSHIHOUTOU 9.0g/d (3M~2Y)

Sponsors

Faculty of Medical Sciences University of Fukui
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.age between 20 and under 80 2.Gender: male and female 3.Outpatient only 4.Patients satisfying the diagnostic criteria for pulmonary MAC disease) A.Clinical criteria (satisfy the following two) 1.Chest CT findings indicate nodular shadow or branched shadow, cavitary shadow, bronchiectasis findings. 2.Can exclude other diseases B.Bacteriological criteria (satisfies one) 1.Culture positive with two or more different sputum 2.Positive cultures in one or more bronchial lavage fluids 3.For transbronchial lung biopsy or lung biopsy tissue, histology findings conformed with pulmonary MAC disease and at the same time tissue or bronchial lavage fluid or sputum one or more culture positive The above A and B are satisfied. 5. Rifampicin, ethambutol, clarithromycin, streptomycin, kanamycin, rifabutin, sitafloxacin, levofloxacin were not administered more than 14 days. 6. Patients who got informed consent.

Exclusion criteria

Exclusion criteria: 1.Rifampicin, ethambutol, clarithromycin, streptomycin, kanamycin, rifabutin, sitafloxacin, levofloxacin are administered 2.Treated for pulmonary tuberculosis 3.With hypokalemia 4.With heart failure 5.With drug hypersensitivity 6.Pregnant and lactating women 7.Patients who participated in other clinical trials within 4 months 8.In addition, patients who are judged inappropriate.

Design outcomes

Primary

MeasureTime frame
CAT score, body weight and NK cell activity on administration and 3 months later.

Secondary

MeasureTime frame
Evaluation of exacerbation factors for exacerbation group and non-exacerbation group Depression score by SDS, STAI Chest CT findings Evaluation of exacerbation factors for exacerbation group and non-exacerbation group evaluation of safety

Countries

Japan

Contacts

Public ContactYuko Waseda

Faculty of Medical Sciences University of Fukui Third Department of Internal Medicine

yuwaseda@mgmail.com0776-61-8355

Outcome results

None listed

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