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Clopidogrel Hyper-Responsiveness: Incidence and Associated Outcomes in Patients With Cerebral Aneurysms

Cerebral Aneurysm Clinical Trial

Official title:
Clopidogrel Hyper-Responsiveness: Incidence and Associated Outcomes in Patients With Cerebral Aneurysms

Clinical Trial Summary

This registry study will investigate the incidence of and outcomes associated with clopidogrel hyper-responsive patients treated at Methodist Dallas Medical Center, beginning in January 2018, who suffered cerebral aneurysms.

Clinical Trial Description

This registry study will investigate the incidence of and outcomes associated with clopidogrel hyper-responsive patients treated at Methodist Dallas Medical Center, beginning in January 2018, who suffered cerebral aneurysms. Perioperative and short-term clinical data will be obtained from electronic medical records. All the data variables will be documented in an Excel sheet (Appendix B). This section will provide an overview of the data collected which will include, but are not limited to, the following: • Pre-Operative Information: Demographics (e.g., age, gender), patient characteristics (e.g., BMI, American Society of Anesthesiologists class), and pre-operative medical history (e.g., tobacco use; comorbidities: hypertension, cardiopulmonary disease, diabetes; etc.). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05945563
Study type Observational [Patient Registry]
Source Methodist Health System
Contact Colette N Ndjom, MS
Phone 214-947-1280
Email MHSIRB@mhd.com
Status Recruiting
Phase
Start date January 17, 2023
Completion date December 17, 2025
View Details
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