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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 weeks
Treatment ~ Varies
Follow Up ~24 hours, 48 hours, 72 hours
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 hours, 48 hours, 72 hours for reporting.

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 • NCT02950558
13%
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

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~0 spots leftby Apr 2025