Cyclosporine A Plus Low-steroid Treatment in COVID-19 Pneumonia
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
1 other identifier
interventional
200
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_1
Started Sep 2020
Shorter than P25 for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2020
CompletedFirst Submitted
Initial submission to the registry
September 2, 2020
CompletedFirst Posted
Study publicly available on registry
September 7, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2020
CompletedSeptember 7, 2020
September 1, 2020
Same day
September 2, 2020
September 4, 2020
Conditions
Outcome Measures
Primary Outcomes (1)
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.
28 days.
Study Arms (1)
COVID-19 Pneumonia control group
EXPERIMENTALCOVID-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.
Interventions
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.
Eligibility Criteria
You may qualify if:
- Confirmed COVID 19 pneumonia by clinical, lung computed Tomography and RT-PCR nasopharyngeal swabs.
You may not qualify if:
- Influenza infection.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Jose Luis Jl Galvez-Romero
Puebla City, 72570, Mexico
Related Publications (49)
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PMID: 32376613RESULT
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
JOSE LUIS J GALVEZ-ROMERO, MD
Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SEQUENTIAL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Master in Medical Sciences and Reasearch and Medical Doctor
Study Record Dates
First Submitted
September 2, 2020
First Posted
September 7, 2020
Study Start
September 1, 2020
Primary Completion
September 1, 2020
Study Completion
September 30, 2020
Last Updated
September 7, 2020
Record last verified: 2020-09
Data Sharing
- IPD Sharing
- Will not share