MedTrace Logo

Opiate Sparing Versus Opiate Based Following Shoulder Arthroplasty

NCT04294680 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 82

Last updated 2022-12-06

Study results available
· View outcomes & findings →

Summary

To investigate the difference between an opiate sparing pain management protocol versus a standard opiate-based protocol following shoulder arthroplasty in the ninety day postoperative period regarding visual analog scores and oral morphine equivalents.

Conditions

  • Shoulder Surgery

Interventions

DEVICE

Cryotherapy

see opiate sparing description

Sponsors & Collaborators

  • Campbell Clinic

    lead OTHER

Principal Investigators

  • Tyler Brolin, MD · Campbell Clinic

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-01
Primary Completion
2021-05-31
Completion
2021-05-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04294680 on ClinicalTrials.gov