Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04355741
Other study ID # COVID19_Microbiota
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 20, 2020
Est. completion date July 16, 2020

Study information

Verified date August 2020
Source Universidade Nova de Lisboa
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Elderly, hypertension, diabetes and cardiovascular diseases are risk factors for COVID-19 morbility and mortality. However, the real reason for this is not yet understood. It is well documented that gut microbiota has a critical role in health, particularly in the immune system and therefore, we propose that gut microbiota composition could affect vulnerability and disease outcomes of COVID-19.


Description:

In order to explore this hypothesis, we will analyse the gut microbiota of SARSCoV-2 infected patients categorized according to location: [1] ambulatory (self-isolation at home), [2] ward and [1] ICU; and severity.


Recruitment information / eligibility

Status Completed
Enrollment 115
Est. completion date July 16, 2020
Est. primary completion date July 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adults of 18 years and above.

- COVID-19 patients.

Exclusion Criteria:

- None.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exposure
Individuals with SARS-CoV-2 exposure and COVID-19 symptoms.

Locations

Country Name City State
Portugal Hospital CUF Infante Santo, S.A. Lisbon
Portugal Hospital de São Francisco Xavier Lisbon
Portugal Centro Hospitalar Universitário São João Oporto

Sponsors (8)

Lead Sponsor Collaborator
Universidade Nova de Lisboa Centro de Medicina Laboratorial Germano de Sousa, S.A., Centro Hospitalar Universitário São João, CINTESIS - Center for Health Technology and Services Research, CUF Academic and Research Medical Center, Hospital CUF Infante Santo, S.A., Hospital de São Francisco Xavier, Centro Hospitalar de Lisboa Ocidental, NOVA Medical School of Universidade NOVA de Lisboa

Country where clinical trial is conducted

Portugal, 

Outcome

Type Measure Description Time frame Safety issue
Primary Differences in gut microbiota composition between COVID-19 patients with different degrees of disease severity. Stool samples of COVID-19 patients will be collected after subject enrollment (single point collection)
Secondary Differences in gut microbiota composition between COVID-19 patients in relation to mortality. Through study completion, an average of 3 months.
Secondary Differences in gut microbiota composition between COVID-19 patients in relation to length of stay in hospitals. Through study completion, an average of 3 months.
Secondary Differences in gut microbiota composition between COVID-19 patients in relation to duration of mechanical ventilation. Through study completion, an average of 3 months.
See also
  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 NCT04481633 - Efficacy of Pre-exposure Treatment With Hydroxy-Chloroquine on the Risk and Severity of COVID-19 Infection N/A
Recruiting NCT05323760 - Functional Capacity in Patients Post Mild COVID-19 N/A
Completed NCT04537949 - A Trial Investigating the Safety and Effects of One BNT162 Vaccine Against COVID-19 in Healthy Adults Phase 1/Phase 2
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
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
Withdrawn NCT05621967 - Phonation Therapy to Improve Symptoms and Lung Physiology in Patients Referred for Pulmonary Rehabilitation N/A
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
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