NCT07773155

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for phase_4

Timeline
4mo left

Started Mar 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress83%
Mar 2025Feb 2027

Study Start

First participant enrolled

March 17, 2025

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

August 14, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 19, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2027

Last Updated

August 19, 2026

Status Verified

August 1, 2026

Enrollment Period

1.9 years

First QC Date

August 14, 2026

Last Update Submit

August 14, 2026

Conditions

Keywords

Wrist Surgery, Hand Surgery, Pain Management

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

EXPERIMENTAL

Regional Nerve Block + Ketorolac (Toradol) + Tylenol (acetaminophen)

Drug: Toradol

Opioid

ACTIVE COMPARATOR

Regional Nerve Block + Oxycodone (5mg, 10 tablets) + Tylenol (acetaminophen)

Drug: Oxycodone

Interventions

Regional Nerve Block + Toradol + Acetaminophen

Non-Opioid

Regional Nerve Block + Oxycodone + Acetaminophen

Opioid

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

MeSH Terms

Conditions

Agnosia

Interventions

Ketorolac TromethamineOxycodone

Condition Hierarchy (Ancestors)

Perceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

IndomethacinIndolesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingHeterocyclic CompoundsCodeineMorphine DerivativesMorphinansOpiate AlkaloidsAlkaloidsHeterocyclic Compounds, Bridged-RingHeterocyclic Compounds, 4 or More RingsPhenanthrenesPolycyclic Aromatic HydrocarbonsPolycyclic Compounds

Central Study Contacts

Jennifer Wolf, MD

CONTACT

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

Locations