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NCT05512546 Clinical Trial

The Prevention of Thromboembolic Complications Associated With Coil Embolization

Prevention Clinical Trial

Official title:
Coil Embolization and Thromboembolic Complications in Patients With Ruptured Aneurysms

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05512546
Other study ID # Lahore General Hospital
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 10, 2017
Est. completion date December 10, 2020

Study information
Verified date August 2022
Source Shaheed Zulfiqar Ali Bhutto Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 200
Est. completion date December 10, 2020
Est. primary completion date February 10, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 45 Years to 80 Years
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Aspir-Low Pill
patients were prescribed 75 mg/day of either aspirin

Locations
Country Name City State
Pakistan Umair Rasheed Lahore Punjab

Sponsors (1)
Lead Sponsor Collaborator
Muhammad Hassan

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary High Intensity Areas post procedural at 24 hours
Primary High Intensity Areas Post Procedural 3 months
Secondary High Intensity Areas Post procedural at 6 months
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