Periarticular Injection Versus Popliteal Block

• Status: Enrolling by invitation
• Trial end date: 2025-07-01
• Target enrollment: 0
• Participant gender: All

Summary

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.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Campbell Clinic
• Treatments: Bupivacaine

Criteria

Inclusion Criteria:

• 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

Exclusion Criteria:

• 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