Inducing and Relieving Factors of Chest Tightness (Pain) in Patients With Acute Coronary Syndrome
NCT ID: NCT07142733
Last Updated: 2025-08-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
142 participants
OBSERVATIONAL
2024-04-01
2025-04-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Retrospective Study of Acute Chest Pain in Extremely Critical Condition for More Than Ten Years
NCT02837120
The Evaluation and Management of Patients With Acute Chest Pain in China
NCT02384863
Usefulness of Chest Wall Tenderness as Bedside Test to Exclude Acute Coronary Syndrome in Different Demographic Groups
NCT01724996
Clinical Features, Treatment Mode and Health Outcomes of Chest Pain Patients in China (CHANGE)
NCT04014972
Non-contrast Cardiac CT as a Risk Stratification Tool in Patients With Non-cardiac Chest Pain
NCT02422316
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* The inclusion criteria for this study comprise patients aged 18 years or older who are proficient in communicating with the researcher in Mandarin or Taiwanese Hokkien.
Exclusion Criteria:
* Exclusion criteria include individuals currently diagnosed with a mental illness, those with substance abuse or alcohol addiction, and those experiencing acute onset symptoms without a prior history of chest discomfort or pain related to heart issues.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Taiwan University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Hsien-Li Kao
Role: STUDY_CHAIR
manager and staff
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Republic of China
Taipei, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
202402091RIND
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.