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AMPED Outcomes Registry of Post-ED Pain Management

NCT01626235 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 843

Last updated 2014-03-12

No results posted yet for this study

Summary

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

Conditions

  • Soft Tissue Injuries
  • Gouty Arthritis
  • Fractures
  • Ureteral Colic
  • Dysmenorrhea

Sponsors & Collaborators

  • American Regent, Inc.

    collaborator INDUSTRY

  • Radnor Registry Research, Inc

    lead INDUSTRY

Principal Investigators

  • Charles V Pollack, MD · University of Pennsylvania

  • Knox Todd, MD · MD Anderson

  • Debra Diercks, MD · UC Davis

  • Sharon Mace, MD · The Cleveland Clinic

  • Stephen Thomas, MD · Univ Oklahoma

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-07-31
Primary Completion
2014-03-31
Completion
2014-03-31

Countries

  • United States

Study Locations

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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 NCT01626235 on ClinicalTrials.gov