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Efficacy and Safety of Qishen Yiqi Dropping Pills in Patients With Severe Pulmonary Hypertension

18 maj 2026 uppdaterad av: XuYu He, Guangdong Provincial People's Hospital

Efficacy and Safety of Qishen Yiqi Dropping Pills in Patients With Severe Pulmonary Hypertension: A Prospective, Randomized Controlled Trial

This study aims to compare the effectiveness and safety of two treatment approaches for patients with severe pulmonary hypertension: standard targeted drug therapy alone, and a combination of standard targeted drugs plus Qishen Yiqi Dropping Pills over 52 weeks of treatment.

Pulmonary hypertension is a chronic condition that raises blood pressure in the lung arteries, causing symptoms like shortness of breath, tiredness, and difficulty with physical activity. While targeted drug treatments are available, many patients still experience persistent symptoms and reduced quality of life. This study will enroll patients with severe pulmonary hypertension to see if adding Qishen Yiqi Dropping Pills to standard treatment can improve patient outcomes.

Participants will be randomly assigned to one of two groups: the combination treatment group will receive Qishen Yiqi Dropping Pills plus standard targeted drugs, and the control group will receive standard targeted drugs alone. All participants will be followed for 52 weeks, during which we will regularly assess:

  • Changes in daily quality of life
  • How far participants can walk in 6 minutes, and their level of breathlessness after the walk
  • Changes in heart function and related blood test indicators
  • Any side effects or discomfort during treatment The primary goal of this study is to see if the combination treatment can improve patients' exercise capacity and quality of life more effectively than standard treatment alone. We will also monitor the safety of adding Qishen Yiqi Dropping Pills to standard therapy. All study procedures follow ethical regulations, and participants can withdraw from the study at any time without affecting their regular medical care.

Studieöversikt

Detaljerad beskrivning

A single-center, parallel, randomized, controlled trial will be conducted to evaluate the efficacy and safety of Qishen Yiqi Dropping Pills combined with western medicine therapy compared with western medicine therapy alone in Asian patients with pulmonary hypertension. A total of 120 pulmonary hypertension patients aged 18-75 years will be recruited into the study in Guangdong Provincial People's Hospital. After a screening period of no more than 2 weeks, patients will be randomly assigned to the Qishen Yiqi Dropping Pills 0.5g three times daily plus targeted drug therapy group or the targeted drug therapy alone group in a 1:1 ratio. All patients in both groups will receive treatment for 52 weeks, and participants will be followed for 26 weeks after the end of treatment. The primary outcomes are the changes in patients' quality of life score, 6-minute walk distance, and Borg score.

Studietyp

Interventionell

Inskrivning (Beräknad)

120

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studieorter

    • Guagdong
      • Guangzhou, Guagdong, Kina, 515000
        • Rekrytering
        • Guangdong Provincial People's Hospital
        • Kontakt:

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

Inclusion Criteria:

  • 1. Male or female participants aged between 18 and 75 years (inclusive) at the screening visit.

    2. Diagnosed with pulmonary arterial hypertension (PAH) classified according to the *2021 Chinese Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension*, and belonging to one of the following subgroups:

  • Subgroup Ⅰ: Idiopathic pulmonary arterial hypertension (IPAH) under the category of arterial pulmonary hypertension
  • Subgroup Ⅱ: Pulmonary hypertension secondary to left heart disease (congenital heart disease) 3. World Health Organization (WHO) Functional Class III or IV symptoms at screening.

    4. Meet all of the following hemodynamic criteria confirmed by right heart catheterization (RHC) at study screening: mean pulmonary arterial pressure (mPAP) ≥ 25 mmHg and pulmonary capillary wedge pressure (PCWP) ≤ 15 mmHg.

    5. Able to walk a minimum of 100 meters and a maximum of 440 meters during the 6-Minute Walk Test (6MWT) at the screening visit; in addition, participants must demonstrate stable baseline 6MWT performance between the screening visit and the randomization visit.

    6. Participants with pulmonary hypertension who are either treatment-naïve or currently receiving treatment: for participants who have received prior treatment (defined as having used PAH-targeted therapeutic agents within 4 weeks before screening), mPAP ≥ 25 mmHg and PCWP ≤ 15 mmHg must be confirmed at the randomization visit.

    7. Able to understand study procedures, willing to comply with study restrictions, and willing and able to provide written informed consent prior to the initiation of all study-related procedures.

Exclusion Criteria:

  • 1. Meet any of the following criteria: 2. Diagnosed with Group 3 or Group 5 pulmonary hypertension (PH) according to the *2021 Chinese Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension*.

    3. Echocardiogram within 6 months before screening indicates left ventricular ejection fraction (LVEF) ≤ 40%, or clinically significant ischemic mitral or aortic valve disease, or constrictive heart disease as judged by the investigator.

    4. Presence of 3 or more of the following risk factors for left ventricular dysfunction:

  • Body mass index (BMI) ≥ 30 kg/m² at screening visit
  • History of essential hypertension
  • Diabetes mellitus of any type
  • History of significant coronary artery disease (CAD) confirmed by any of the following:
  • History of myocardial infarction
  • History of percutaneous coronary intervention (PCI)
  • Angiographic evidence of ≥ 50% stenosis in at least one major coronary artery
  • Positive cardiac stress imaging test
  • History of coronary artery bypass graft surgery (CABG)
  • History of chronic stable angina or unstable angina 5. Uncontrolled systemic arterial hypertension: systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 110 mmHg at randomization visit (Day 1).

    6. History of long QT syndrome or torsades de pointes ventricular tachycardia. 7. Serum alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥ 3 times the upper limit of normal (ULN) at screening visit.

    8. Severe renal impairment: estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m² at screening calculated by the CKD-EPI formula.

    9. Severe hepatic impairment (Child-Pugh Class C) at screening visit, with or without cirrhosis; patients receiving renal dialysis or with a history of renal transplantation.

    10. Known coagulation defects, including: hereditary or acquired coagulation disorders (factor XII deficiency, factor XIII deficiency), reduced coagulation factor production due to acute or chronic liver disease, impaired coagulation efficiency caused by lupus anticoagulant, disseminated intravascular coagulation (DIC), or anticoagulant factor autoantibodies.

    11. Evidence or history of major hemorrhage or intracranial hemorrhage. 12. History of increased intracranial pressure. 13. Pregnant or lactating women. 14. Any surgical or medical condition that may significantly alter the absorption, distribution, metabolism, or excretion of any drug, including but not limited to: history of major gastrointestinal surgery deemed clinically significant by the investigator within 12 months before screening (e.g., gastrectomy, gastrointestinal stoma anastomosis, intestinal resection, gastric bypass surgery, gastroenterostomy, or gastric banding), current active inflammatory bowel disease, or history of active inflammatory bowel disease.

    15. Any surgical or medical condition not specified in the protocol that, in the investigator's opinion, would expose the patient to higher risk due to study participation, or may prevent the patient from complying with study requirements or completing the trial period.

    16. Patients who are unwilling or unable to safely discontinue current pulmonary arterial hypertension (PAH)-targeted medications during the study as required by the protocol.

    17. History of any contraindication or hypersensitivity reaction to any study drug or drugs with similar chemical structures.

    18. History of active substance abuse (including alcohol) within the past 1 year, or patients considered potentially unreliable by the investigator.

    19. Personnel directly involved in the conduct of this clinical study.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Dubbel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Active Comparator: QSYQ Pills + targeted monotherapy group
Patients in this arm will receive a 12-week period of Qishen Yiqi Dropping Pills 0.5g orally three times daily (tid) in combination with targeted monotherapy.

Experimental Group: Qishen Yiqi Dropping Pills combined with standard PAH-targeted therapy.

Qishen Yiqi Dropping Pills is an NMPA-approved Chinese patent medicine for cardiovascular diseases, each pill is 0.5g, main ingredients include astragalus membranaceus, salvia miltiorrhiza, panax notoginseng and dalbergia odorifera. Administration: 0.5g orally tid after meals.

Targeted therapy follows *2021 Chinese PAH Diagnosis and Treatment Guidelines*, including one or more approved PAH-targeted agents at clinically recommended doses. Total treatment duration: 26weeks.

Aktiv komparator: Active Comparator: targeted monotherapy group
Patients in this arm will receive a 12-week period of targeted monotherapy.

Control Group Intervention: Participants in this group receive standard pulmonary arterial hypertension (PAH)-targeted therapy alone, without additional Qishen Yiqi Dropping Pills.

The targeted therapy regimen complies with the *2021 Chinese Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension*, including one or more clinically approved PAH-targeted agents (endothelin receptor antagonists, phosphodiesterase type 5 inhibitors, or soluble guanylate cyclase stimulators) at standard recommended doses. The regimen is consistent with the participants' stable pre-enrollment treatment plan, or initiated per the protocol-specified dosing schedule, with no dose adjustment allowed during the study period unless required for safety reasons. The total treatment duration is 26 weeks, identical to the experimental group.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change from Baseline in 6-Minute Walk Distance (6MWD) at 52 Weeks
Tidsram: Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks, 52weeks (end of treatment)
The 6-Minute Walk Test (6MWT) is a standardized, objective measure of functional exercise capacity commonly used in cardiovascular disease populations. Participants will be instructed to walk as far as possible on a flat, 30-meter long corridor for a total duration of 6 minutes, with the total distance covered (in meters) recorded as the 6-Minute Walk Distance (6MWD). The change in 6MWD from baseline to the end of the treatment period will be calculated as the primary efficacy endpoint, with a greater increase indicating better improvement in cardiopulmonary function and exercise tolerance.
Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks, 52weeks (end of treatment)
Change from Baseline in Seattle Angina Questionnaire (SAQ) Score at 52 Weeks
Tidsram: Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks, 52weeks (end of follow-up)
The Seattle Angina Questionnaire (SAQ) is a validated, disease-specific quality of life measure for patients with cardiovascular disease, covering 5 domains: physical limitation, angina stability, angina frequency, treatment satisfaction, and disease perception. Each domain score ranges from 0 to 100, with higher scores indicating better health status and less symptom burden. The change in total SAQ score from baseline to the end of follow-up will be calculated as the primary efficacy endpoint.
Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks, 52weeks (end of follow-up)
Change from Baseline in Borg Rating of Perceived Exertion (RPE) Scale Score at 52 Weeks
Tidsram: Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks,52weeks (end of follow-up)
The Borg Rating of Perceived Exertion (RPE) Scale is a widely used, validated self-report measure of subjective exercise intensity and dyspnea in cardiovascular patient populations. The 6-20 point Borg Scale will be administered immediately after the 6-Minute Walk Test, where participants rate their perceived level of exertion ranging from 6 (no exertion at all) to 20 (maximal exertion). Lower scores indicate less perceived physical exertion and better exercise tolerance. The change in Borg RPE score from baseline to the end of treatment will be calculated as the primary efficacy endpoint.
Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks,52weeks (end of follow-up)

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change from Baseline in N-Terminal Pro-B-Type Natriuretic Peptide (NT-proBNP) Concentration at 52 Weeks
Tidsram: Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks, 52weeks (end of follow-up)

N-terminal pro-B-type natriuretic peptide (NT-proBNP) is a well-validated circulating biomarker for cardiac wall stress, ventricular dysfunction, and cardiovascular disease prognosis, widely used in the management of heart failure, acute coronary syndrome and other cardiovascular conditions.

Fasting venous blood samples will be collected from participants at specified time points, and serum NT-proBNP concentration will be measured using a clinically validated quantitative assay (unit: picograms per milliliter, pg/mL). The change in NT-proBNP concentration from baseline to the end of treatment will be calculated as the primary efficacy endpoint: a greater reduction in NT-proBNP indicates alleviation of cardiac load and better therapeutic effect.

For participants with heart failure, a reduction of ≥30% in NT-proBNP from baseline is generally recognized as a threshold of clinically meaningful improvement.

Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks, 52weeks (end of follow-up)
Change from Baseline in WHO (NYHA) Functional Classification of Cardiac Status at 52 Weeks
Tidsram: Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks,52weeks (end of follow-up)

The World Health Organization (WHO) recommended New York Heart Association (NYHA) Functional Classification is a widely used, validated clinical scale to assess the severity of heart failure and functional status in patients with cardiovascular disease. The classification grades cardiac function based on the degree of dyspnea and fatigue experienced during daily activities, ranging from Grade I to Grade IV:

  • Grade I: No limitation of physical activity; ordinary physical activity does not cause undue fatigue, dyspnea, or palpitations.
  • Grade II: Slight limitation of physical activity; comfortable at rest, but ordinary physical activity results in symptoms of fatigue, dyspnea, or palpitations.
  • Grade III: Marked limitation of physical activity; comfortable at rest, but less than ordinary activity causes symptoms.
  • Grade IV: Unable to carry out any physical activity without symptoms; symptoms of heart failure are present even at rest, and any physical exertion increases discomfort.

T

Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks,52weeks (end of follow-up)
Change from Baseline in Systolic Pulmonary Arterial Pressure (sPAP) Measured by Echocardiography at 12 Weeks
Tidsram: Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks,52weeks (end of follow-up)

Systolic Pulmonary Arterial Pressure (sPAP) is a key hemodynamic parameter reflecting the pressure in the pulmonary artery during cardiac systole, widely used for the diagnosis, severity assessment and prognosis evaluation of pulmonary hypertension, left heart failure, valvular heart disease and other cardiovascular conditions.

sPAP will be measured by transthoracic echocardiography performed by qualified sonographers at specified time points, calculated based on the tricuspid regurgitation jet velocity using the simplified Bernoulli equation, with measurement unit in millimeters of mercury (mmHg). The change in sPAP concentration from baseline to the end of treatment will be calculated as the primary efficacy endpoint: a greater reduction in sPAP indicates alleviation of pulmonary vascular resistance and right ventricular load, as well as better therapeutic effect.

In patients with left heart disease related pulmonary hypertension, a reduction of ≥10 mmHg in sPAP from baseline is gen

Baseline, 1 weeks, 8 weeks, 26 weeks,40weeks,52weeks (end of follow-up)
Incidence of Adverse Events (AEs) and Serious Adverse Events (SAEs) in Participants Receiving Qishen Yiqi Dropping Pills Combined with Targeted Therapy versus Targeted Therapy Alone
Tidsram: Baseline (within 7 days before treatment initiation), every 2 weeks during treatment, at the end of treatment (12 weeks), and 30 days after the last dose of study treatment (safety follow-up)
Baseline (within 7 days before treatment initiation), every 2 weeks during treatment, at the end of treatment (12 weeks), and 30 days after the last dose of study treatment (safety follow-up)

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Studieavstämningsdatum

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Studera stora datum

Studiestart (Faktisk)

25 oktober 2023

Primärt slutförande (Beräknad)

30 juni 2030

Avslutad studie (Beräknad)

31 december 2030

Studieregistreringsdatum

Först inskickad

18 maj 2026

Först inskickad som uppfyllde QC-kriterierna

18 maj 2026

Första postat (Faktisk)

22 maj 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

22 maj 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

18 maj 2026

Senast verifierad

1 maj 2026

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