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81mg aspirin for Postoperative Complications
N/A
Waitlist Available
Led By Joseph M Vitello, MD
Research Sponsored by Jesse Brown VA Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up intraoperative only
Awards & highlights
Study Summary
The purpose of this study is to determine whether aspirin taken in the perioperative period will increase the blood loss associated with open inguinal hernia repairs. A secondary purpose of this study is to determine if the aspirin administered in the perioperative period increases the risk of complications associated with open inguinal hernia repairs.
Eligible Conditions
- Postoperative Complications
- Inguinal Hernia
- Postoperative Hemorrhage
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 30 days post operative
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days post operative
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
intraoperative blood loss
Secondary outcome measures
Number of Participants with Serious and Non-Serious Adverse Events
Trial Design
2Treatment groups
Experimental Treatment
Group I: 81mg aspirinExperimental Treatment1 Intervention
This arm will include perioperative 81 mg of aspirin.
Group II: 325mg aspirinExperimental Treatment1 Intervention
Subjects will be taking 325mg of aspirin.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Acetylsalicylic acid
FDA approved
Find a Location
Who is running the clinical trial?
Jesse Brown VA Medical CenterLead Sponsor
7 Previous Clinical Trials
1,615 Total Patients Enrolled
Joseph M Vitello, MDPrincipal InvestigatorJesse Brown VA Medical Center
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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