Covid-19 Clinical Trial
Official title:
Association of the Neutrophil/Lymphocyte Ratio and Lymphocyte /Platelet Ratio With Clinical Complications and Mortality in COVID-19 Patients
NCT number | NCT04434157 |
Other study ID # | NR-09-2020 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 28, 2020 |
Est. completion date | May 5, 2020 |
Verified date | June 2020 |
Source | Hospital Regional de Alta especialidad de Ixtapaluca |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
There is little information about the clinical characteristics and risk factors of Covid-19
in Latin American countries considering the ethnic differences and the high prevalence of
obesity and cardiometabolic diseases. The aim of the study was to evaluate the association
between laboratory tests and the risk of complications in SARS-CoV-2 infection and to
determine their mortality risk factors in a sample of the Mexican population.
A retrospective cross-sectional study of the routinely collected data was performed in the
Hospital Regional de Alta Especialidad de Ixtapaluca (HRAEI), State of Mexico. Adult patients
(aged ≥18 years) with positive RT-PCR for SARS-CoV-2 and oxygen support that were admitted
between March 28 and May 5, 2020, were included
Status | Completed |
Enrollment | 221 |
Est. completion date | May 5, 2020 |
Est. primary completion date | May 5, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: 1. Adult patients (aged =18 years) 2. Clinical (Positive RT-PCR for SARS-CoV-2 test) and radiological diagnosis of pulmonary infection by COVID-19 3. Diagnosis of acute respiratory distress syndrome clinical panel in accordance with Berlin 2012 criteria 4. Need of non-invasive ventilation (NIV or CPAP) or invasive ventilation (intubation) Exclusion Criteria: 1. Previous diagnosis of severe liver or kidney failure. 2. Patients with Human Immunodeficiency Virus (HIV) infection. 3. Patients with previous hematological diseases (Leukemia) that condition alterations in blood counts. 4. Consumption of treatments with any type of immunosuppressants prior to admission that conditions low lymphocytes. 5. Patients with a diagnosis of active or non-active cancer. 6. Absence of a clinical record for monitoring the data. 7. Pregnancy. 8. Patients referred from other institutions for their medical care. Clinical records of patients who requested their voluntary discharge Clinical records that do not include information of the course of COVID-19 infection |
Country | Name | City | State |
---|---|---|---|
Mexico | Hospital Regional de Alta Especialidad de Ixtapaluca | Ixtapaluca | State Of Mexico |
Lead Sponsor | Collaborator |
---|---|
Hospital Regional de Alta especialidad de Ixtapaluca | Hospital General de México Dr. Eduardo Liceaga |
Mexico,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Hematic and biochemical parameters | To evaluate the differences in hematic and biochemical parameters between survivors and no survivors | 10 days | |
Other | Chronic diseases | To identify the chronic diseases in the patientss´medical records associated with the pulmonary complications | 10 days | |
Primary | Clinical complications and Mortality | To main aim of the study is to evaluate clinical complicatios and mortality in mexican Covid-19 patients | 10 days | |
Primary | Neutrophil-Lymphocyte and Lymphocyte-Platelet ratio | To evaluate the association of the hematological ratios with the clinical complicatios and mortality in covid-19 patinets | 10 days |
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT06065033 -
Exercise Interventions in Post-acute Sequelae of Covid-19
|
N/A | |
Completed |
NCT06267534 -
Mindfulness-based Mobile Applications Program
|
N/A | |
Completed |
NCT05047601 -
A Study of a Potential Oral Treatment to Prevent COVID-19 in Adults Who Are Exposed to Household Member(s) With a Confirmed Symptomatic COVID-19 Infection
|
Phase 2/Phase 3 | |
Recruiting |
NCT05323760 -
Functional Capacity in Patients Post Mild COVID-19
|
N/A | |
Recruiting |
NCT04481633 -
Efficacy of Pre-exposure Treatment With Hydroxy-Chloroquine on the Risk and Severity of COVID-19 Infection
|
N/A | |
Completed |
NCT04612972 -
Efficacy, Safety and Immunogenicity of Inactivated SARS-CoV-2 Vaccines (Vero Cell) to Prevent COVID-19 in Healthy Adult Population In Peru Healthy Adult Population In Peru
|
Phase 3 | |
Completed |
NCT04537949 -
A Trial Investigating the Safety and Effects of One BNT162 Vaccine Against COVID-19 in Healthy Adults
|
Phase 1/Phase 2 | |
Recruiting |
NCT05494424 -
Cognitive Rehabilitation in Post-COVID-19 Condition
|
N/A | |
Active, not recruiting |
NCT06039449 -
A Study to Investigate the Prevention of COVID-19 withVYD222 in Adults With Immune Compromise and in Participants Aged 12 Years or Older Who Are at Risk of Exposure to SARS-CoV-2
|
Phase 3 | |
Enrolling by invitation |
NCT05589376 -
You and Me Healthy
|
||
Completed |
NCT05158816 -
Extracorporal Membrane Oxygenation for Critically Ill Patients With COVID-19
|
||
Recruiting |
NCT04341506 -
Non-contact ECG Sensor System for COVID19
|
||
Completed |
NCT04512079 -
FREEDOM COVID-19 Anticoagulation Strategy
|
Phase 4 | |
Completed |
NCT04384445 -
Zofin (Organicell Flow) for Patients With COVID-19
|
Phase 1/Phase 2 | |
Completed |
NCT05975060 -
A Study to Evaluate the Safety and Immunogenicity of an (Omicron Subvariant) COVID-19 Vaccine Booster Dose in Previously Vaccinated Participants and Unvaccinated Participants.
|
Phase 2/Phase 3 | |
Active, not recruiting |
NCT05542862 -
Booster Study of SpikoGen COVID-19 Vaccine
|
Phase 3 | |
Terminated |
NCT05487040 -
A Study to Measure the Amount of Study Medicine in Blood in Adult Participants With COVID-19 and Severe Kidney Disease
|
Phase 1 | |
Withdrawn |
NCT05621967 -
Phonation Therapy to Improve Symptoms and Lung Physiology in Patients Referred for Pulmonary Rehabilitation
|
N/A | |
Terminated |
NCT04498273 -
COVID-19 Positive Outpatient Thrombosis Prevention in Adults Aged 40-80
|
Phase 3 | |
Active, not recruiting |
NCT06033560 -
The Effect of Non-invasive Respiratory Support on Outcome and Its Risks in Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-COV-2)-Related Hypoxemic Respiratory Failure
|