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Evaluation of the Renal Function in an Ultra-endurance Race. (INFERNAL)

C

Central Hospital, Nancy, France

Status

Completed

Conditions

Renal Insufficiency, Acute

Treatments

Other: INFERNAL Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT03136315
2017-A00808-45

Details and patient eligibility

About

During ultra endurance events, athletes experience extreme physical and mental demands, sometimes at the limits of the adaptive response to human physiology. This is particularly true for the renal function, and some evidence for acute renal failure has already been shown, sometimes leading to dialysis. However, the precise mechanisms involved in acute renal failure in such ultra endurance races are not clearly elucidated.

The aim of our study is to estimate glomerular filtration rate from serum and urinary creatinine and cystitin C at the beginning and at the end of a 110 km ultra endurance race. Our hypothesis is that during the ultra endurance race, renal function may be injured, with a risk for the athlete.

Enrollment

54 patients

Sex

All

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age: At least 20 years old
  • Athlete that is officially registered to the 110 km race (INFERNAL Trail des Vosges)
  • Athlete informed by a member (MD) of the Medical Staff of the race.
  • Athlete that gives and signes the informed consent to the research protocol

Exclusion criteria

  • Athlete with a known disease that needs the following medications:
  • Medications influencing the renin-angiotensin-aldosteron system (angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, aldosteron receptor blockers)
  • Diuretic drugs
  • Anticoagulant drugs
  • Non-steroidal anti-inflammatory drugs
  • Athlete with a known thyroid disease (because of the influence on the serum cystatin level)
  • Athlete with a know renal disease
  • Athlete with a know inflammatory disease

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

54 participants in 1 patient group

INFERNAL Arm
Experimental group
Description:
The INFERNAL Arm will have serum and urinary dosage for creatinine and cystanin C at the beginning and at the end of the 110 km race.
Treatment:
Other: INFERNAL Intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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