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Pupil Response in Patients on Opioids.

NCT02247024 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 63

Last updated 2019-01-29

No results posted yet for this study

Summary

Evaluation of pupillary reflex in patients on high-dose opioids. Clinical assessment of pain intensity, sedation score, and other side effects of opioids. Measurements of the concentration of opioids and their active metabolites in blood.

Conditions

  • Chronic Pain
  • Impaired Pupillary Reflex
  • Opioid-Related Disorders

Sponsors & Collaborators

  • Oslo University Hospital

    lead OTHER

Principal Investigators

  • Ulf E Kongsgaard, MD PhD · Oslo University Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2018-08-31
Completion
2018-11-30

Countries

  • Norway

Study Locations

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Entities

Diseases

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 NCT02247024 on ClinicalTrials.gov