Optimal Management of Pain in Hospitalized Patients - Opioid Tolerant Populations.
Pain, Acute Pain, Postoperative Pain
About this trial
This is an interventional health services research trial for Pain focused on measuring patient readmission, pain relief units, pain centers, multidisciplinary pain clinics, multidisciplinary pain centers, pain clinics, hospital readmission, emergencies, emergency medicine, critical care, emergency treatment, opioid, acute pain service
Eligibility Criteria
Inclusion Criteria:
- Adult patients (18 years and older)
- Known opioid tolerant (as determined per FDA criteria)
- Agree to sign the informed consent and HIPAA forms
Exclusion Criteria:
- Patients under the age of 18 years
- No known opioid tolerance
- Do not agree to sign the informed consent and HIPAA forms
Sites / Locations
- University of California, Irvine Medical Center
- Duke University Medical Center
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Control Group
Treatment Group
Those randomized into the control group will receive the current standard of care for pain management. This standard care pathway involves a pain management specialist consultation only at the request of the primary admitting team. The pain management consultation can occur at any time during the patient's inpatient stay and care by these specialists ends at discharge.
Subjects randomized into the treatment (early intervention) group will receive the New Clinical Pathway: pain management care coordinated by pain-management specialists from inpatient admission through 60 days after discharge.