GERONIMO 19: NORMAL HUMAN IMMUNOGLOBULINS (IVIG) IN PATIENTS AGED 75 YEARS AND OVER, COVID-19 WITH SEVERE ACUTE RESPIRATORY FAILURE

Sponsor
Versailles Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT04403269
Collaborator
(none)
35
1
1
12
2.9

Study Details

Study Description

Brief Summary

According to recent data, death rate is more than 20% for 75 years old hospitalized patients and older.

In case of aggravation, according to the latest observations, if they are refused for mechanical ventilation in intensive care, their death rate could reach 60% even for patients without comorbidity.

Apart from an increase in oxygen therapy, no specific treatment is currently proposed.

The control of the inflammatory component seems to be a key element to be able to influence the patients' health evolution.

Polyvalent intravenous immunoglobilins have immunomodulatory and anti-inflammatory properties with a favorable safety profile for these elderly patients and several clinical cases lead to positive impact in the caring for Covid patients.

This study objective is evaluation of the efficacy of polyvalent IVIg in combination with the standard management of patients aged 75 and over with SARSCov2 infection with acute respiratory failure (saturation ≤ 95%) requiring oxygen therapy> 5 L / min (i.e. patients considered as moderate to severe ARDS according to the Berlin definition, Pa02 / Fi02≤200) and disqualified from a care in the ICU.

Condition or Disease Intervention/Treatment Phase
Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
35 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
"STUDY OF THE EFFICIENCY OF NORMAL HUMAN IMMUNOGLOBULINS (IVIG) IN PATIENTS AGED 75 YEARS AND OVER COVID-19 WITH SEVERE ACUTE RESPIRATORY FAILURE" GERONIMO 19
Actual Study Start Date :
May 5, 2020
Anticipated Primary Completion Date :
May 5, 2021
Anticipated Study Completion Date :
May 5, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: IgIV

The experimental arm is human immunoglobulins. 2 infusion at D1 and D2. (0.8 g / kg by IV infusion)

Drug: IgIV
2 infusion at D1 and D2 (0.8 g / kg by IV infusion)

Outcome Measures

Primary Outcome Measures

  1. Mortality [Day 14]

Secondary Outcome Measures

  1. Total number of days of full hospitalization [3 and 6 months]

  2. Duration of oxygen therapy [3 and 6 months]

  3. Ferritin level in the blood [3 and 6 months]

  4. CRP level in the blood [3 and 6 months]

  5. LDH level in the blood [3 and 6 months]

  6. Lymphocyte level in the blood [3 and 6 months]

  7. PNN level in the blood [3 and 6 months]

  8. platelet level in the blood [3 and 6 months]

  9. WHO performance index [3 and 6 months]

  10. WHOQOL-OLD questionnaire [3 and 6 months]

  11. Lung function by pulmonary computed tomography [3 and 6 months]

  12. Lung function by EFR [3 and 6 months]

  13. Mortality [3 and 6 months]

  14. Readmission Rates [3 and 6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
75 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Man or woman aged 75 and over

  • SARS-coV2 infection confirmed by RT-PCR or thoraco-pulmonary CT

  • Hospitalized in the acute general geriatrics unit of the Versailles Hospital Center

  • Patient rejected from resuscitation

  • Saturation ≤ 95% under oxygen therapy> 5 L / min (i.e. PaO2 / FiO2≤200mmHg according to the Berlin definition of ARDS) by means of a nasal cannula, a high concentration facial mask or another device similar oxygen distribution

Exclusion Criteria:
  • Patient under palliative care

  • Patient with contraindication to IV polyvalent Ig

  1. . Hypersensitivity to the active substance or to any of the excipients (L-proline)

  2. . Hypersensitivity to human immunoglobulins, especially when the patient has anti-IgA antibodies,

  3. . Patients with type I or II hyperprolinemia

  • Patient under guardianship or curatorship

  • Patient receiving another experimental treatment as part of an interventional study

  • Moderate to severe dementia known: it must have been diagnosed before hospitalization and is defined by an MMSE <20/30 or a neuropsychological assessment with a diagnosis made.

  • Patient not affiliated with a social security system in France

  • ADL patients <4/6 and / or IADL <6/8

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre Hospitalier de Versailles Le Chesnay France 78150

Sponsors and Collaborators

  • Versailles Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr Laure PARNET, Principal Investigator, Versailles Hospital
ClinicalTrials.gov Identifier:
NCT04403269
Other Study ID Numbers:
  • P20/07 GERONIMO 19
First Posted:
May 27, 2020
Last Update Posted:
May 27, 2020
Last Verified:
May 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 27, 2020