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Search / Trial NCT06636318

Immune Status After Being on Call for 24 Hrs

Launched by UNIVERSITY OF CHICAGO · Oct 9, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying how staying awake for 24 hours affects the immune system, particularly in surgery residents who often work long shifts without sleep. Researchers want to understand if being sleep-deprived leads to an increase in inflammation and a decrease in the body’s ability to fight off infections. The results could help shed light on how sleep deprivation impacts health, especially for those in demanding medical careers.

To participate in this study, individuals need to be healthy surgery residents aged 18 or older, regardless of gender or background. They must be able to give consent to join the trial. Participants will undergo assessments to examine their immune cells and how they function after a long shift, alongside some health measurements. This study aims to gather important information that could improve the well-being of medical professionals who frequently face sleep deprivation.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Healthy subjects
  • Surgery residents in a 24-hour shift rotation
  • Gender of subjects: Males and females
  • Age of subjects: 18 years old and older
  • Racial and Ethnic Origin: Any race or ethnicity
  • Exclusion Criteria:
  • Unwilling/unable to sign informed consent
  • Vulnerable Subjects/Subject Capacity to provide consent

About University Of Chicago

The University of Chicago is a prestigious research institution renowned for its commitment to advancing medical science through innovative clinical trials. With a robust infrastructure that supports multidisciplinary collaboration, the University actively engages in cutting-edge research across various therapeutic areas. Its dedicated team of experienced investigators and state-of-the-art facilities enable the University of Chicago to conduct rigorous clinical studies aimed at improving patient outcomes and translating scientific discoveries into tangible healthcare solutions. The institution prioritizes ethical standards and patient safety, ensuring that all trials adhere to the highest regulatory guidelines and best practices in clinical research.

Locations

Chicago, Illinois, United States

Patients applied

0 patients applied

Trial Officials

Angelica Perez-Gutierrez, MD

Principal Investigator

University of Chicago

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported