A Study Demonstrating that the ExSpiron Monitor Provides Data on Patients at Risk Recovering From Surgery

Overview

About this study

The purpose of this study is to assess the benefit to patients of continuous respiratory monitoring using the ExSpiron System in the post-anesthesia environment.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria

  • Patients ≥ 21 years of age
  • Undergoing non-emergent surgery with general anesthesia
  • Planned transfer to the PACU after surgery
  • Able to give informed consent.

 

Exclusion Criteria

  • Patients not able to give informed consent
  • Inability to place the PadSets on the thorax
  • Existence of an active implanted neurostimulator.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Jacksonville, Fla.

Mayo Clinic principal investigator

Stephen Aniskevich, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Additional contact information

Non-cancer trials contact form

Phone: 800-664-4542 (toll-free)

International patient clinical studies questions