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Effect of Shufeiya Prescription on Pulmonary Artery Systolic Pressure and Quality of Life in Patients with Pulmonary Hypertension

Effect of Shufeiya Prescription on Pulmonary Artery Systolic Pressure and Quality of Life in Patients with Pulmonary Hypertension

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046512
Enrollment
Unknown
Registered
2021-05-18
Start date
2021-06-01
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

Pulmonary Hypertension

Interventions

Sponsors

The First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 80 years, gender is not limited; 2.Meets the diagnostic standard of pulmonary hypertension; 3.Patients with fixed dose and type of conventional medicine last month; 4.Patients who did not receive targeted drug therapy or targeted drug therapy regimen fixed for at least a month; 5.Patients who had not received interventional or surgical treatment within 6 months before the trial; 6.Volunteer to participate in the clinical trial, understand and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with acute exacerbation of chronic heart failure, acute myocardial infarction, coronary revascularization, and cardiac resynchronization within a month before the trial; 2.Patients with acute exacerbation of COPD/combined pulmonary infection within a month before the trial; 3.Patients with right ventricular outflow tract obstruction; 4.Patients with malignant tumors, mental disorders, malignant arrhythmias and other serious diseases; 5.Patients with severe renal disease (serum creatinine > 450umol/L) or liver disease (including serum transaminase >3 times the upper limit of normal value); 6.Patients who had taken Chinese medicine preparations (including TCM decoction pieces, granules, Proprietary Chinese medicine, TCM intravenous preparations, etc.) within 2 weeks before the trial; 7.Patients with disadvantageous activities of lower limbs and unable to cooperate with the completion of relevant examinations; 8.Pregnant women and lactating women; 9.Patients with known allergy to the drug ingredients and excipients in this trial.

Design outcomes

Primary

MeasureTime frame
Pulmonary artery systolic pressure;

Secondary

MeasureTime frame
Six minutes walking distance;WHO functional class;Borg dyspnea scores;Ultrasonic cardiogram;Quality of Life Scale;Endothelin - 1;Nitric oxide;

Countries

China

Contacts

Public ContactMao Jingyuan

The First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

jymao@126.com+86 13820498886

Outcome results

None listed

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