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Truncal blocks for Intraoperative Pain
N/A
Waitlist Available
Led By Ali Shariat, MD
Research Sponsored by Icahn School of Medicine at Mount Sinai
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 up to post-op day 10
Awards & highlights
Study Summary
This study is evaluating whether local anesthetic infiltration or truncal blocks are better for pain control after S-ICD implantation.
Eligible Conditions
- Intraoperative Pain
- Postoperative Pain
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to post-op day 10
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to post-op day 10
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Intraoperative and postoperative opioid consumption
Secondary outcome measures
Duration of ICU stay
Length of stay
Non-opioid analgesic consumption
+4 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Truncal blocksExperimental Treatment1 Intervention
Truncal block for anesthetics
Group II: Wound infiltrationActive Control1 Intervention
Standard intervention - surgical infiltration with local anesthetics
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Truncal blocks
2019
N/A
~30
Find a Location
Who is running the clinical trial?
Icahn School of Medicine at Mount SinaiLead Sponsor
861 Previous Clinical Trials
525,252 Total Patients Enrolled
Ali Shariat, MDPrincipal InvestigatorIcahn School of Medicine at Mount Sinai
3 Previous Clinical Trials
53 Total Patients Enrolled
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