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Nerve block for Ankle Surgery
N/A
Waitlist Available
Led By Glenn G Shi, MD
Research Sponsored by Mayo Clinic
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 24 hours, 48 hours, 72 hours
Awards & highlights
Study Summary
This study is evaluating whether a high ankle block during ankle surgery provides the same pain relief as the standard regional block.
Eligible Conditions
- Ankle Surgery
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 hours, 48 hours, 72 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours, 48 hours, 72 hours
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in pain score
Side effects data
From 2020 Phase 4 trial • 14 Patients • NCT0295055813%
wound dehiscence
100%
80%
60%
40%
20%
0%
Study treatment Arm
Standard Care
Ropivacaine Pump
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: High ankle blockExperimental Treatment1 Intervention
High ankle block for acute pain control after elective ankle surgery
Group II: Single shot regional popliteal and saphenous blockActive Control1 Intervention
Standard of care traditional single shot popliteal / saphenous regional block for acute pain control after elective ankle surgery
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Nerve block
2016
Completed Phase 4
~450
Find a Location
Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,205 Previous Clinical Trials
3,766,784 Total Patients Enrolled
1 Trials studying Ankle Surgery
21 Patients Enrolled for Ankle Surgery
Glenn G Shi, MDPrincipal InvestigatorMayo Clinic
1 Previous Clinical Trials
178 Total Patients Enrolled
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