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Study on the clinical efficacy and safety of Maxing Xiongting Mixture in the treatment of COPD patients with hypoxia-pulmonary hypertension with phlegm and blood stasis syndrome based on the theory of heart-lung co-treatment

Study on the clinical efficacy and safety of Maxing Xiongting Mixture in the treatment of COPD patients with hypoxia-pulmonary hypertension with phlegm and blood stasis syndrome based on the theory of heart-lung co-treatment

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076932
Enrollment
Unknown
Registered
2023-10-24
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-10-30

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

Conditions

COPD with hypoxia-pulmonary hypertension

Interventions

Experimental group:Maxing Xiongting Mixture and Western medicine treatment

Sponsors

Chongqing Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) The patients with COPD complicated with pulmonary hypertension are in stable stage, and have no respiratory tract infection and acute attack of chronic obstructive pulmonary disease in the past 4 weeks; (2) It conforms to the syndrome of phlegm and blood stasis; (3) Age = 40 years old and<80 years old, regardless of gender; (4) The dose and type of conventional western medicine treatment drugs are fixed in the past month; (5) Not receiving targeted drug treatment; (6) The patient or family member is willing to sign an informed consent form and participate in the study.

Exclusion criteria

Exclusion criteria: (1) Pulmonary hypertension caused by other chronic lung diseases (interstitial lung disease, pneumoconiosis, sleep apnea, etc.) or other reasons; (2) Pregnant women and lactating women; (3) Those who are allergic to the study drug; (4) It is accompanied by serious heart, liver and kidney system diseases or connective tissue diseases in active stage; (5) Patients with right ventricular outflow tract obstruction; (6) Those who lack informed consent or patients do not cooperate and cooperate; (7) Participate in other clinical researchers.

Design outcomes

Primary

MeasureTime frame
Pulmonary artery systolic pressure;

Secondary

MeasureTime frame
Pulmonary function;Cardiac color Doppler echocardiography;6min walk test;Borg Dyspnea Score;WHO functional classification;TCM syndrome score;Quality of life scale;HIF-1a;ET-1;NO;NT-proBNP;

Countries

China

Contacts

Public ContactXing An

Chongqing Traditional Chinese Medicine Hospital

xing_an1995@163.com+86 136 8813 8502

Outcome results

None listed

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