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Renal Considerations in the Heat Stress Recommendations (Aim2)

Indiana University logo

Indiana University

Status

Completed

Conditions

Hot Weather; Adverse Effect
Dehydration
Hyperthermia
Kidney Injury
Kidney Dysfunction

Treatments

Procedure: No fluid replacement
Procedure: Fluid replacement

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

An epidemic of chronic kidney disease is occurring in laborers who undertake physical work outdoors in hot conditions. The reason for this is largely unknown, but may be related to kidney dysfunction caused by increases in body temperature and dehydration that elicit oxidative stress and inflammation in the renal tubules. The purpose of this study is to determine whether hydration status modifies the development of renal oxidative stress and inflammation.

Enrollment

18 patients

Sex

All

Ages

18 to 44 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Men and women
  • 18-44 y old
  • Body mass index ≤35.0 kg/m2
  • Self-reported to be healthy

Exclusion criteria

  • Not within defined age range
  • Estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73m2
  • Body mass index >35.0 kg/m2
  • Current or history of any renal disease, heart disease, stroke, immune or autoimmune disease, and/or gastrointestinal disease/surgery
  • Hypertension during screening (systolic blood pressure >139 or diastolic blood pressure >89)
  • Using medications that blunt the physiological response to exercise (e.g., beta blockers)
  • Prescription medication with a known side effect of impaired temperature regulation or fluid balance (e.g., diuretics)
  • Positive pregnancy test at any time during the study or breast feeding
  • Current tobacco or electronic cigarette use or consistent use within the last 2 years
  • Answered "Yes" to any question on Page 1 of the PAR-Q+.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

18 participants in 2 patient groups

Fluid replacement
Experimental group
Treatment:
Procedure: Fluid replacement
No fluid replacement
Sham Comparator group
Treatment:
Procedure: No fluid replacement

Trial contacts and locations

1

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Central trial contact

Zachary J Schlader, PhD

Data sourced from clinicaltrials.gov

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