# Perioperative Pain Management for Total Shoulder Arthroplasty: A Pilot Non-Inferiority Trial

> **NCT05908851** · NA · UNKNOWN · sponsor: **London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's** · enrollment: 80 (estimated)

## Conditions studied

- Shoulder Arthritis
- Anesthesia, Local
- Local Infiltration

## Interventions

- **DRUG:** 100 mL of 0.9% normal saline (57ml), 0.5% ropivacaine (40 ml), 10 mg morphine (10 mg/ml), 0.1 mg of epinephrine (0.1 mg/ml), and 30 mg of ketorolac (30 mg/ml)

## Key facts

- **NCT ID:** NCT05908851
- **Lead sponsor:** London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2023-11-01
- **Primary completion:** 2024-11-01
- **Final completion:** 2025-11-01
- **Target enrollment:** 80 (ESTIMATED)
- **Last updated:** 2023-10-05


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05908851

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05908851, "Perioperative Pain Management for Total Shoulder Arthroplasty: A Pilot Non-Inferiority Trial". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT05908851. Licensed CC0.

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