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CompletedNCT04587375Dyhor-19Updated Oct 14, 2020

Diagnosis of Endocrine Dysfunctions in Covid-19

An observational study in Covid 19, sponsored by University Hospital, Montpellier. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-10-14.

Sponsored by University Hospital, Montpellier · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

As observed with SARS-CoV responsible for SARS 2003, the new coronarovirus SARS-CoV-2 uses the angiotensin converting enzyme type 2 (ACE2) as cellular receptor to infect cells. The renin aldosterone angiostensin system (RAAS) has known effects in the lungs: some receptors are pro-inflammatory, others are anti-inflammatory. Thus the deregulation of the RAAS induced by the SARS-CoV-2 could explain the inflammatory response of Covid-19 infection and be a modulator of the severity of its course.

Furthermore, the SARS 2003 experience suggests that there may be others endocrine involvment, particularly an failure on the hypothalamus-pituitary and adrenal axis. Indeeed, cases of hypocorticism and hypothyroidism of central origin were described.

Altogether, the endocrine system might play a role both in the pathophysiology of Covid-19 infection and in the activity and severity of the disease.

In this study, the investigators proposed to explore endocrine functions on biological samples in a series of patients admitted for Covid-19 in our clinic.

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Conditions studied

  • Covid 19

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Keywords

  • Covid-19
  • Renin Angiotensin Aldosterone System
  • Hormon disorders
03

In context

COVID-19

7,640 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's enrollment of 50 is below the median of 260 across 3,135 observational studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with Covid-19 diagnosis hospitalized in Montpellier University hospital

Inclusion criteria

  • Patients with Covid-19 diagnosis and hospitalized in our clinic

Exclusion criteria

Exclusion criteria:

  • Minor patient
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Plasma aldosterone levels

    Plasma aldosterone levels

    Time frame: 1 day (at inclusion)

  2. Plasma renin levels

    Plasma renin levels

    Time frame: 1 day (at inclusion)

Secondary outcomes

  1. covid-19 infection severity

    covid-19 infection severity : Ordinal scale of 7 values from 1 to 7 (1- not hospitalized, no limitation on activities; 2- not hospitalized, limitations on activities; 3- hospitalized, not requiring supplemental oxygen; 4- hospitalized, requiring supplemental oxygen; 5- hospitalized, on non-invasive ventilation or high flow oxygen devices; 6- hospitalized, on invasive mechanical ventilation or ECMO and 7- death).

    Time frame: 1 day (at inclusion)

  2. Maximum severity of Covid-19 infection

    Maximum severity of Covid-19 infection using a seven-category ordinal scale at at the end of hospitalization : Ordinal scale of 7 values from 1 to 7 (1- not hospitalized, no limitation on activities; 2- not hospitalized, limitations on activities; 3- hospitalized, not requiring supplemental oxygen; 4- hospitalized, requiring supplemental oxygen; 5- hospitalized, on non-invasive ventilation or high flow oxygen devices; 6- hospitalized, on invasive mechanical ventilation or ECMO and 7- death).

    Time frame: 1 day (at inclusion)

  3. Plasma aldosterone level

    Plasma aldosterone level

    Time frame: 1 day (at the end of hospitalization)

  4. Plasma ACTH level

    Plasma ACTH level

    Time frame: 1 day (at the end of hospitalization)

  5. Plasma cortisol level

    Plasma cortisol level

    Time frame: 1 day (at inclusion)

  6. Plasma cortisol level

    Plasma cortisol level

    Time frame: 1 day (at the end of hospitalization)

  7. Plasma T3l level

    Plasma T3l level

    Time frame: 1 day (at the end of hospitalization)

  8. Plasma T3l level

    Plasma T3l level

    Time frame: 1 day (at inclusion)

  9. Plasma ACTH level

    Plasma ACTH level

    Time frame: 1 day (at inclusion)

  10. Plasma LH level

    Plasma LH level

    Time frame: 1 day (at inclusion)

  11. Plasma LH level

    Plasma LH level

    Time frame: 1 day (at the end of hospitalization)

  12. Plasma DHEA level

    Plasma DHEA level

    Time frame: 1 day (at the end of hospitalization)

  13. Plasma DHEA level

    Plasma DHEA level

    Time frame: 1 day (at inclusion)

  14. Plasma estradiol (female) or testosterone (male) level

    Plasma estradiol (female) or testosterone (male) level

    Time frame: 1 day (at the end of hospitalization)

  15. Plasma estradiol (female) or testosterone (male) level

    Plasma estradiol (female) or testosterone (male) level

    Time frame: 1 day (at inclusion)

  16. Plasma FSH level

    Plasma FSH level

    Time frame: 1 day (at the end of hospitalization)

  17. Plasma FSH level

    Plasma FSH level

    Time frame: 1 day (at inclusion)

  18. type of treatments

    type of treatments

    Time frame: 1 day

  19. Clinical characteristics

    Clinical characteristics extracted from electronic medical

    Time frame: 1 day

  20. radiological characteristics

    radiological characteristics : quantification of the percentage of lesional damage to the pulmonary parenchyma

    Time frame: 1 day

07

Study locations

1 site
  • Uhmontpellier
    Montpellier, 34295, France
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References and documents

Individual participant data

Plan to share: Undecided — NC

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 14, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04587375
Lead sponsor
University Hospital, Montpellier
Responsible party
Sponsor
First posted
Oct 14, 2020
Start date
Mar 1, 2020
Primary completion
May 1, 2020
Completion
May 30, 2020
Last update
Oct 14, 2020

Study contacts

Philippe GUILPAIN, MD, PhD
study director · University Hospital, Montpellier

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2020. You cannot join it, but the record below documents what was studied.

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