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

NCT02630134 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 6

Last updated 2017-07-18

No results posted yet for this study

Summary

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

Conditions

  • Pain Measurement
  • Assessment, Pain

Interventions

OTHER

These patients receive the Baeta device and take it home

Sponsors & Collaborators

Principal Investigators

  • Michael Haile, MD · NYU School of Medicine

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2011-06-30
Completion
2012-10-31

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT02630134 on ClinicalTrials.gov