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NCT06699420RecruitingPhase 4

Qishenyiqi Dripping Pill for Coronary Microvascular Disease

The Efficacy and Safety of Qishenyiqi Dripping Pill in Patients With Coronary Microvascular Disease

Source: ClinicalTrials.gov · Last updated 21 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

To investigate the efficacy and safety of Qishenyiqi in patients with microvascular angina pectoris. Long-term follow-up of 1 year will be performed to evaluate the effect of Qishenyiqi on coronary flow reserve and adverse cardiovascular events in patients with coronary microvascular disease.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
162 (estimated)
First submitted
18 Nov 2024
Start date
8 Nov 2023
Primary completion date
31 Dec 2025
Lead sponsor
Qilu Hospital of Shandong University
NCT number
NCT06699420

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 162
  • From 8 Nov 2023 to the primary completion date, 31 Dec 2025
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous myocardial infarction or PCI or CABG treatment;
  • Patients who participated in clinical research of other drugs within 3 months before being selected.

Other illness

  • A history of heart failure;
  • Severe arrhythmia;
  • Refractory hypertension or hypertension accompanied by left ventricular wall thickness \> 12 mm;
  • Takayasu arteritis, Kawasaki disease or coronary artery malformation;
  • Allergic to contrast agents or traditional Chinese medicines;

Other

  • Familial hypercholesterolemia;
  • Pregnant or nursing, or having the intention to give birth within one year;
  • Hepatic or renal dysfunction;

Who the study is looking for

  • Repeated chest pain attacks with typical exertional angina pectoris or resting angina pectoris attacks;
  • Coronary normal or stenosis \< 20%;
  • Ischemic depression in ST segment during resting or exercise;
  • Blood flow reserve (CFR) of the anterior descending coronary artery \< 2.0;
  • Subjects or their guardians agreed to participate in this study.

Age in the registry: 40 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Qilu Hospital of Shandong University
Coordinator of this site? Confirm its status
JinanChinaRecruiting
Qianfoshan Hospital, Shandong University
Coordinator of this site? Confirm its status
JinanChinaActive, not recruiting
Jinan Central Hospital Affiliated to Shandong First Medical University
Coordinator of this site? Confirm its status
JinanChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.