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Real-world Study on Clinical Characteristics and Risk Factors of Ticagrelor-related Dyspnea

Real-world Study on Clinical Characteristics and Risk Factors of Ticagrelor-related Dyspnea

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116220
Enrollment
Unknown
Registered
2026-01-07
Start date
2026-01-13
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Coronary heart disease

Interventions

Dyspnea Group:None

Sponsors

Chinese Academy of Medical Sciences Peking Union Medical College TEDA International Cardiovascular Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients aged >= 18 years with coronary heart disease who were hospitalized in our hospital and treated with ticagrelor from January 2019 to January 2025 were enrolled;

Exclusion criteria

Exclusion criteria: 1.With a history of respiratory diseases, such as chronic obstructive pulmonary disease (COPD), bronchial asthma, pulmonary embolism, acute respiratory distress syndrome (ARDS), etc. 2.Cardiac insufficiency [left ventricular ejection fraction (LVEF) < 40% or New York Heart Association (NYHA) functional classification grade ? or above]; 3.Severe hepatic and renal dysfunction [Child-Pugh classification grade C, estimated glomerular filtration rate (eGFR) < 30 mL/(min•1.73 m²)]; 4.Active peptic ulcer or gastrointestinal bleeding; 5.A history of hemorrhagic stroke within the past 6 months;

Design outcomes

Primary

MeasureTime frame
Whether dyspnea occurred;

Countries

China

Contacts

Public ContactRuihua Wang

Chinese Academy of Medical Sciences Peking Union Medical College TEDA International Cardiovascular Hospital

Ruihua371519@163.com+86 22 65208048

Outcome results

None listed

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