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.