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OpenTrials
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NCT Number: NCT07835009

Burnout Among Cardiac Anaesthesiology and Cardiac Surgery Residents

To evaluate autonomic nervous system disturbances with respect to Ansiscope in cardiac anaesthesia residents in 24hrs shift.

Why the study stopped: Principal Investigator (PI) is not available to continue further
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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Sri Jayadeva Institute of cardiovascular Science and Research

Bengaluru, Karnataka, 560069, India

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Resident doctors with a minimum of one year experience in cardiac anaesthesia.
  • Resident doctors with a minimum of one year experience in cardiac surgery.

Exclusion criteria

  • Residents not consenting for the study Data loss or data unavailability

Treatment and study plan

ANSiscope

Device

Resident doctors with a minimum of one year experience in cardiac anaesthesia on 24hrs shift are chose and then the ANSiScope measurement is taken as per the designed procedure.

Primary outcomes

  1. Stress Analysis

    Time frame: 2 weeks

    Analysis of stress in cardiac anaesthesia residents in 24hrs shift.

Sponsors and collaborators

Lead sponsor

DyAnsys, Inc.

Industry

Registry information

Official study title

Burnout Among Cardiac Anaesthesiology and Cardiac Surgery Residents: Is it a Hidden Health Care Crisis?

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Sep 22, 2026
Registry last updated
Sep 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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