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Clinical Trials/NCT05512546
NCT05512546CompletedNot Applicable

Coil Embolization and Thromboembolic Complications in Patients With Ruptured Aneurysms

Muhammad Hassan1 site in 1 country200 target enrollmentStarted: February 10, 2017Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
High Intensity Areas

Study Overview

Brief Summary

Clopidogrel has been to be reported to be superior to aspirin for the prevention of thromboembolic complications associated with coil embolization in patients with ruptured aneurysms.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Retrospective

Eligibility Criteria

Ages
45 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • All the patients enrolled in the study underwent MRI and Angiography.
  • Participants included in the study were confirmed on assessment, and verified for ruptured aneurysm by imaging using either computed tomography (CT) or MRI.

Exclusion Criteria

  • Patients with any history of sensitivity or reaction to aspirin, or any contraindication for MRI, were excluded from the study.

Arms & Interventions

Aspirin Group

patients were prescribed 75 mg/day of either aspirin for 6 months

Intervention: Aspir-Low Pill (Drug)

Clopidogrel Group

75mg/day prescribed for 6 months

Intervention: Aspir-Low Pill (Drug)

Outcomes

Primary Outcomes

High Intensity Areas

Time Frame: 3 months

Post Procedural

Secondary Outcomes

  • High Intensity Areas(at 6 months)

Investigators

Sponsor
Muhammad Hassan
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Muhammad Hassan

Registrar Neurology

Shaheed Zulfiqar Ali Bhutto Medical University

Study Sites (1)

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