Clinical Trials Directory

Trials / Unknown

UnknownNCT05945563

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

Status
Unknown
Phase
Study type
Observational
Enrollment
208 (estimated)
Sponsor
Methodist Health System · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Accepted

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.

Detailed 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.).

Conditions

Timeline

Start date
2023-01-17
Primary completion
2025-01-17
Completion
2025-12-17
First posted
2023-07-14
Last updated
2024-03-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05945563. Inclusion in this directory is not an endorsement.