Clinical Trial: AMPED Outcomes Registry of Post-ED Pain Management

Study Status: Completed
Recruit Status: Completed
Study Type: Observational

Official Title: Acute Management of Pain From the Emergency Department: A National, Emergency Department-Based Prospective Post-Intervention Registry of Non-Opioid and Opioid Management of Acute Pain

Brief Summary: Study aims to assess patient-recorded outcomes of pain control medications prescribed in the ER after visits for specific painful injuries/illnesses.

Detailed Summary: Multicenter, observational, prospective, out-of-hospital registry collecting clinical, satisfaction, quality of life, and healthcare resource utilization from subjects discharged after ED care for a specific acute pain syndrome with a clinician-determined analgesic regimen. Subjects are stratified by diagnosis and by regimen based on the treating clinician's judgment. The registry study is independent of ED care and clinician's decision-making.
Sponsor: Radnor Registry Research, Inc

Current Primary Outcome: Clinical Outcomes of pain control measures [ Time Frame: 5 days ]

  1. Change in pain score over follow-up interval;
  2. Healthcare resource utilization during follow-up interval;
  3. Patient satisfaction with therapy;
  4. Return to work in employed cohort.


Original Primary Outcome: Same as current

Current Secondary Outcome: Satisfaction and Economic Outcomes [ Time Frame: 5 days ]

  1. Effectiveness of work upon return;
  2. Relative adverse effect profiles of three treatment regimens;
  3. Compliance with therapy;
  4. QOL at conclusion of therapy.


Original Secondary Outcome: Same as current

Information By: Radnor Registry Research, Inc

Dates:
Date Received: June 20, 2012
Date Started: July 2012
Date Completion:
Last Updated: March 11, 2014
Last Verified: March 2014