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A randomized control trial of Hotyuekkito in patients with chronic obstructive pulmonary disease who receive pulmonary rehabilitation

A randomized control trial of Hotyuekkito in patients with chronic obstructive pulmonary disease who receive pulmonary rehabilitation - A randomized control trial of Hotyuekkito in patients with chronic obstructive pulmonary disease who receive pulmonary rehabilitation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000015092
Enrollment
40
Registered
2014-09-08
Start date
2014-09-08
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

chronic obstructive pulmonary disease

Interventions

Hotyuekkito is administrated in patients with chronic obstructive pulmonary disease who receive pulmonary rehabilitation Hotyuekkito is not administrated in patients with chronic obstructive pulmonary

Sponsors

Hiroshima University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)COPD stage 2-3, FEV1/FVC<70%,30%<FEV1 pred<70% 2)Clinically stable COPD 3)No reciving pulmonary rehabilitation within 24 weeks 4)Ideal body weight <100% 5)Age: 40 years or older 6)Smoking history > 10 pack-years 7)Male or female 8)Patients who will be able to receive treatment for 12 weeks 9)Written informed consent

Exclusion criteria

Exclusion criteria: 1)Diagnosed other pulmonary diseases 2)No acute exacervation within 4 weeks 3)Receiving pulmonary transplantation 4)Receiving herbal medicine within 4 weeks 5)Receiving inhaled or systemic steroid therapy within 2 weeks 6)Engage other clinical trial within 4 weeks 7)alpha1 antitrypsin deficiency 8)Severe other diseases such as malignancy, autoimmune disease, liver disease, renal disease, heart disease, hematologic disease, and metabolic disease 9)Pregnant and nursing 10)Inappropriate patients

Design outcomes

Primary

MeasureTime frame
Six minutes walking test Safety

Secondary

MeasureTime frame
Grasping powergrip, Body weight, Body mass index, Hematological data, Modified Medical Research Council dyspnea scale, Quality of life questionnaire

Countries

Japan

Contacts

Public ContactNoboru Hattori

Hiroshima University Hospital Department of Respiratory Medicine

nhattori@hiroshima-u.ac.jp082-257-5196

Outcome results

None listed

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