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Cyclosporine A Plus Low-steroid Treatment in COVID-19 Pneumonia

Primary Purpose

COVID 19 Pneumonia

Status
Unknown status
Phase
Phase 1
Locations
Mexico
Study Type
Interventional
Intervention
Cyclosporin A
Sponsored by
Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID 19 Pneumonia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Confirmed COVID 19 pneumonia by clinical, lung computed Tomography and RT-PCR nasopharyngeal swabs.

Exclusion Criteria:

  • Influenza infection.

Sites / Locations

  • Jose Luis Jl Galvez-Romero

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

COVID-19 Pneumonia control group

Arm Description

COVID-19 pneumonia patients with standar treatment: enoxaparin 0.5 mg/kg S.C. once, Clarithromycin 500 mg twice an metylprednisolone 0.5 mg/kg once endovenous.

Outcomes

Primary Outcome Measures

Number of days to clinical improvement until hospital discharge or death.
Improvement of patients, defined by the following parameters: lower oxygen requirements (2 liters per minute, or less), absence of fever by three consecutive days, respiratory rate <22, a decrease of 50% or more in the C reactive protein on admission, and length of hospital stay.

Secondary Outcome Measures

Full Information

First Posted
September 2, 2020
Last Updated
September 4, 2020
Sponsor
Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado
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1. Study Identification

Unique Protocol Identification Number
NCT04540926
Brief Title
Cyclosporine A Plus Low-steroid Treatment in COVID-19 Pneumonia
Official Title
Utility of Low Doses of Corticosteroids and Cyclosporine Combined With Enoxaparin, in Patients With COVID-19 Pneumonia at the ISSSTE Regional Hospital, Puebla, During the Contingency Period Due to the SARS-Cov2 Pandemic
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Unknown status
Study Start Date
September 2020 (Anticipated)
Primary Completion Date
September 2020 (Anticipated)
Study Completion Date
September 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Methods: Single-center pilot study included PCR+ SARS-CoV2-patients, hospitalized from April to May 2020 in Puebla, Mexico. Comparative treatment with steroids plus CsA or steroids. Mild, moderate or severe pneumonia was measured by clinical, laboratory tests, lung damage score by computed tomography, and score for clinical improvement. Death rate was evaluated at 28 days.
Detailed Description
This is a pilot study done in a single center (ISSSTE Regional Hospital, Puebla, Mexico). Consecutive patients with suspected or confirmed diagnosis of COVID-19 were assigned, in an unblinded and non-randomized fashion, to receive either steroids plus CsA (intervention group) or steroids only (standard of treatment in this hospital, control group), as per individual clinical judgment. The primary outcome was the number of days to clinical improvement until hospital discharge or death. The secondary outcome was the improvement of patients, defined by the following parameters: lower oxygen requirements (2 liters per minute, or less), absence of fever by three consecutive days, respiratory rate <22, a decrease of 50% or more in the C reactive protein on admission, and length of hospital stay. Adult patients attending to the hospital between April 15, to May 31, 2020, fulfilling symptoms compatible with COVID-19 pneumonia, according to the WHO guidance, were invited to participate and all the patients gave their written informed consent.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID 19 Pneumonia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Sequential Assignment
Model Description
Consecutive patients with suspected or confirmed diagnosis of COVID-19 were assigned, in an unblinded and non-randomized fashion, to receive either steroids plus CsA (intervention group) or steroids only (standard of treatment in this hospital, control group), as per individual clinical judgment
Masking
None (Open Label)
Allocation
N/A
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
COVID-19 Pneumonia control group
Arm Type
Experimental
Arm Description
COVID-19 pneumonia patients with standar treatment: enoxaparin 0.5 mg/kg S.C. once, Clarithromycin 500 mg twice an metylprednisolone 0.5 mg/kg once endovenous.
Intervention Type
Drug
Intervention Name(s)
Cyclosporin A
Intervention Description
COVID-19 pneumonia patients treated with oral CsA at a dose of 1-2 mg /kg / day divided into two doses, for 7 days, since entering to hospitalization.
Primary Outcome Measure Information:
Title
Number of days to clinical improvement until hospital discharge or death.
Description
Improvement of patients, defined by the following parameters: lower oxygen requirements (2 liters per minute, or less), absence of fever by three consecutive days, respiratory rate <22, a decrease of 50% or more in the C reactive protein on admission, and length of hospital stay.
Time Frame
28 days.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed COVID 19 pneumonia by clinical, lung computed Tomography and RT-PCR nasopharyngeal swabs. Exclusion Criteria: Influenza infection.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
JOSE LUIS J GALVEZ-ROMERO, MD
Phone
+522222453511
Ext
1100
Email
jose.galvez@issste.gob.mx
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
JOSE LUIS J GALVEZ-ROMERO, MD
Organizational Affiliation
Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado
Official's Role
Principal Investigator
Facility Information:
Facility Name
Jose Luis Jl Galvez-Romero
City
Puebla
ZIP/Postal Code
72570
Country
Mexico
Facility Contact:
First Name & Middle Initial & Last Name & Degree
JOSE LUIS J GALVEZ-ROMERO
Phone
+522222453511
Ext
1100
Email
jose.galvez@issste.gob.mx

12. IPD Sharing Statement

Plan to Share IPD
No
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Softic L, Brillet R, Berry F, Ahnou N, Nevers Q, Morin-Dewaele M, Hamadat S, Bruscella P, Fourati S, Pawlotsky JM, Ahmed-Belkacem A. Inhibition of SARS-CoV-2 Infection by the Cyclophilin Inhibitor Alisporivir (Debio 025). Antimicrob Agents Chemother. 2020 Jun 23;64(7):e00876-20. doi: 10.1128/AAC.00876-20. Print 2020 Jun 23.
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Cyclosporine A Plus Low-steroid Treatment in COVID-19 Pneumonia

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