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Prospective Cases for Length of Stay
Phase 4
Waitlist Available
Led By Michelle Palazzo, MD
Research Sponsored by Christine M. Kleinert Institute for Hand and Microsurgery
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 120 minutes post-operation
Awards & highlights
Study Summary
This study is evaluating whether a type of pain medicine given before surgery may help reduce pain after surgery.
Eligible Conditions
- Length of Stay
- Postoperative Pain
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 120 minutes post-operation
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~120 minutes post-operation
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Post-operative pain
Secondary outcome measures
Length of Hospital Stay
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Prospective CasesExperimental Treatment1 Intervention
These cases will be recruited prospectively, and receive the intercostal nerve block(s) on operated site(s). Peri-operative injections of 30 ml of 0.25% Bupivacaine each, injected over the 4th, 5th, and 6th ribs on the operated site(s).
Group II: Retrospective ControlsActive Control1 Intervention
Controls will be gathered retrospectively from chart reviews where patient did not receive a intercostal nerve blocker bilaterally.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Bupivacaine
FDA approved
Find a Location
Who is running the clinical trial?
Christine M. Kleinert Institute for Hand and MicrosurgeryLead Sponsor
10 Previous Clinical Trials
925 Total Patients Enrolled
Baptist HealthUNKNOWN
Jewish Hospital and St. Mary's HealthcareOTHER
4 Previous Clinical Trials
909 Total Patients Enrolled
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