Effect of Local Anesthetic Concentration on Rebound Pain: A Randomized Control Study
Starting soon · Phase 4
Conditions studied: Rebound Pain, Shoulder Arthroplasty, Interscalene Block
In brief
Randomized control study that compares different concentrations of local anesthetic to investigate whether a lower concentration of local anesthetic would contribute to lower rebound pain scores at 24 hours post op in patients undergoing anatomic or reverse total shoulder arthroplasty.
Key facts
- Study ID
- NCT07146685
- Run by
- University of Virginia
- People needed
- 168
- Starts
- 2026-01-01
- Expected to finish
- 2029-01-01
- Last updated by the study team
- 2025-08-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Total shoulder replacement patients (anatomic and reverse)
- Adult patients (greater than or equal to 18 years)
- Any gender
- Any race
You may not qualify if…
- - Chronic Pain diagnoses including:
- substance/opioid use disorder
- complex regional pain syndromes
- fibromyalgia
- Daily persistent opioid use spanning 3 months prior to surgery date
- Allergy to local anesthetics or NSAIDS
- Respiratory pathologies including:
- CPAP- non-compliant / untreated obstructive sleep apnea
- COPD
- Restrictive lung disease (pulmonary fibrosis, interstitial pneumonia, etc)
- Contralateral diaphragm dysfunction
- BMI > 40
- Ipsilateral extremity pre-existing nerve injury
- GFR < 60
- NSAID contraindications
- Inability to follow up
- Revision surgery
- Patients requesting block as primary (avoidance of general anesthesia)
- Need or request for brachial plexus catheter or liposomal bupivacaine
- Vulnerable populations (pregnancy, incarceration, etc)
- non-English speaking
Where it is running
- UVA Health — Charlottesville, Virginia, United States
Full record on ClinicalTrials.gov
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