Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06636318

Immune Status After Being on Call for 24 Hrs

Led by University of Chicago · Updated on 2025-12-09

60

Participants Needed

1

Research Sites

162 weeks

Total Duration

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AI-Summary

What this Trial Is About

Sleep deprivation is a prevalent problem in modern societies. Sleep deprivation can cause hormonal changes, such as an increase in cortisol, as well as inflammation. Animal studies have shown an increase in inflammatory cytokine production following sleep deprivation. Additionally, humans experiencing sleep deprivation may experience a decrease in natural killer cells and lymphocytes. Physicians, particularly those in surgical specialties, are often subjected to sleep deprivation as part of their medical residency training. This study hypothesizes that after 24-hour shifts, there is an increase in inflammatory response and impairment of the immune response against unspecific activation. This proposal aims to provide insight into the impact of sleep deprivation on the immune system of surgery residents by characterizing the phenotype and function of immune cells, as well as their correlation with biometric data.

CONDITIONS

Official Title

Immune Status After Being on Call for 24 Hrs

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy subjects
  • Surgery residents in a 24-hour shift rotation
  • Male or female gender
  • Age 18 years and older
  • Any race or ethnicity
Not Eligible

You will not qualify if you...

  • Unable or unwilling to sign informed consent
  • Vulnerable subjects or unable to provide consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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+1

Trial Site Locations

Total: 1 location

1

The University of Chicago

Chicago, Illinois, United States, 60637

Actively Recruiting

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Research Team

A

Angelica Perez-Gutierrez, MD

CONTACT

L

Leila Yazdanbakhsh

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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