Pain Control With Ketorolac and Nerve Block After Wrist and Hand Surgery
A Pilot Study to Assess Pain Control With Ketorolac and Nerve Block After Wrist and Hand Surgery
1 other identifier
interventional
120
1 country
1
Brief Summary
The purpose of this study is to learn about the effectiveness of different pain control options after hand and wrist surgery, specifically Ketorolac, Tylenol, and a regional nerve block. Ketorolac (Toradol) is a nonsteroidal anti-inflammatory drug (NSAID) that is similar to ibuprofen (Motrin or Advil). Tylenol (acetaminophen) is a commonly used over the counter drug. A nerve block is pain medication that is applied directly to the nerves around the surgical site before the surgery and keeps working to reduce pain in the area for several hours after the surgery. All of these medicines and procedures are approved by the Food and Drug Administration (FDA) for patient care. This study aims to understand if using these medicines in combination helps patients having hand and wrist surgery avoid the need for opioid pain medications.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_4
Started Mar 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 17, 2025
CompletedFirst Submitted
Initial submission to the registry
August 14, 2026
CompletedFirst Posted
Study publicly available on registry
August 19, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 1, 2027
August 19, 2026
August 1, 2026
1.9 years
August 14, 2026
August 14, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Postoperative Pain, as measured by the Numeric Pain Scale
The numerical pain rating scale is used for rating postoperative pain. Pain scores rate from 0 to 10, with higher scores indicating more severe pain.
2 days, 1 week and 2 weeks post op
Secondary Outcomes (1)
Opioid requirements, measured in oral morphine equivalents
Through 2 weeks postop
Study Arms (2)
Non-Opioid
EXPERIMENTALRegional Nerve Block + Ketorolac (Toradol) + Tylenol (acetaminophen)
Opioid
ACTIVE COMPARATORRegional Nerve Block + Oxycodone (5mg, 10 tablets) + Tylenol (acetaminophen)
Interventions
Eligibility Criteria
You may qualify if:
- Age 18 years or older
- Undergoing upper extremity surgery performed by a hand and upper extremity orthopaedic surgeon at the University of Chicago.
- Undergoing procedure with regional nerve block
You may not qualify if:
- Age less than 18 years
- Concomitant chronic opioid use
- Postoperative opioid use (surgery through POD 14) for condition other than repaired fracture
- Medical contraindication to ketorolac use, including pregnancy
- Undergoing multiple concurrent surgical procedures
- Unable to communicate numerical pain score
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Chicago
Chicago, Illinois, 60637, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SEQUENTIAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 14, 2026
First Posted
August 19, 2026
Study Start
March 17, 2025
Primary Completion (Estimated)
February 1, 2027
Study Completion (Estimated)
February 1, 2027
Last Updated
August 19, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share
No current plan to share data