Viewing Study NCT07142733


Ignite Creation Date: 2025-12-25 @ 3:00 AM
Ignite Modification Date: 2025-12-26 @ 1:41 AM
Study NCT ID: NCT07142733
Status: COMPLETED
Last Update Posted: 2025-08-27
First Post: 2025-07-16
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Inducing and Relieving Factors of Chest Tightness (Pain) in Patients With Acute Coronary Syndrome
Sponsor: National Taiwan University Hospital
Organization:

Study Overview

Official Title: Inducing and Relieving Factors of Chest Tightness (Pain) in Patients With Acute Coronary Syndrome
Status: COMPLETED
Status Verified Date: 2024-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ACS
Brief Summary: The research aims to investigate various aspects related to chest discomfort (pain) in patients diagnosed with Acute Coronary Syndrome (ACS). Firstly, it seeks to identify the factors that trigger such discomfort in ACS patients. Additionally, the study aims to explore different methods utilized to alleviate chest pain in these individuals and assess their effectiveness. Furthermore, it aims to analyze how basic attributes of patients may influence both the precipitating factors and the effectiveness of relief methods for chest discomfort. Finally, the research aims to understand how factors related to other diseases may impact chest discomfort and its alleviation methods in ACS patients.
Detailed Description: 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 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.

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: