Device for Monitoring Pain During Intraoperative, Pre/Post Surgical Periods: Comparison With Standard of Care Monitoring

Stopped early · Not applicable

Conditions studied: Pain Measurement, Assessment, Pain

In brief

Study patients are given a hand held device to track pain post surgery.

Key facts

Study ID

NCT02630134

Run by

NYU Langone Health

People needed

6

Starts

2011-03-01

Expected to finish

2012-10-01

Last updated by the study team

2017-07-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 or older
• post thoracotomy with a consult placed to the acute pain service on post-op day 0 for management of a PCA or epidural
• mental status permits patient to reliably press a button to record pain or administer medications
• must be hemodynamically stable
• must be able to physically use the MyHealth trends diary (press a button)
• supplies written informed consent.

You may not qualify if…

• less than 18 years of age
• has any underlying or current medical condition, which, in the opinion of the Investigator, would interfere with the use of the MyHealth trends device (e.g. severe psychosis, quadrapalegic, etc.)
• Subject necessitates ICU care

Where it is running

• NYU Langone Medical Center — New York, New York, United States

Full record on ClinicalTrials.gov

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