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Objective Measure of Recovery After Outpatient Surgery

NCT02616406 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 5

Last updated 2022-08-10

No results posted yet for this study

Summary

This is a study using wearable monitoring devices, patient activity and sleep patterns to monitor pre and post operative following outpatient inguinal hernia surgery to determine when these parameters return to baseline.

Conditions

  • Hernia, Inguinal
  • Convalescence

Interventions

DEVICE

GENEactiv

To wear a monitoring device for a period of time prior to surgery and post surgery

Sponsors & Collaborators

  • Arizona State University

    collaborator OTHER

  • Mayo Clinic

    lead OTHER

Principal Investigators

  • Karl A. Poterack, M.D. · Mayo Clinic

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2019-07-31
Completion
2019-07-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT02616406 on ClinicalTrials.gov