Periarticular Injection Versus Popliteal Block

Enrolling by invitation · Phase 4

Conditions studied: Foot Surgery, Ankle Surgery

In brief

This study aims to determine the effectiveness and safety of two standard of care perioperative procedures for controlling pain following ankle and hindfoot osteotomy or fusion or ankle fracture repair.

Key facts

Study ID

NCT04575688

Run by

Campbell Clinic

People needed

100

Starts

2021-07-13

Expected to finish

2027-02-28

Last updated by the study team

2025-12-24

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Ankle or hindfoot osteotomy or ankle fracture repair
• Surgery scheduled at Campbell Surgery Center (1410 Brierbrook Road, Germantown, TN 38138)
• 18-80 years of age
• ASA I-III with medical clearances as needed
• Fluent ub verbal and written English
• Willing and able to comply with study instruction and commit to all follow-up visits for theduration of the study
• Willing and able to provide written consent

You may not qualify if…

• Diagnosed with chronic pain syndrome
• History of allergic reactions to lidocaine, marcaine, Experal, bupivicaine, or other injectable anesthetic agents
• Injury associated with workers' compensation
• Surgery to be performed at a hospital
• Diagnosed with peripheral neuropathy
• Hbg A1C is > 7 mg/dl in diabetic patients only
• Long term (chronic) preoperative narcotic usage

Where it is running

• A — Germantown, Tennessee, United States

Full record on ClinicalTrials.gov

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