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10 clinical studies listed.

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SARS-CoV 2

Tundra lists 10 SARS-CoV 2 clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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COMPLETED

NCT04444596

Conjunctival Swab vs Nasopharyngeal Swab in Patients With COVID-19

The aim of this possible study is to identify if SARS-CoV-2 can be found in the tear film and conjunctiva of a patient with COVID-19.

Gender: All

Ages: 18 Years - Any

Updated: 2026-10-08

1 state

COVID-19
SARS-CoV 2
RECRUITING

NCT04448145

Determinants of SARS (Severe Acute Respiratory Syndrome)-COV2 (COVID-19) Persistence After Convalescence

The 2019-2020 COVID-19 pandemic is the largest outbreak in recent history. It is not known how long after someone gets sick with COVID-19 and recovers that they can still infect other people. It is also not known how quickly people make antibodies against the virus, which help clear infection from the body. The investigators will enroll 300 people who had COVID-19 based on lab testing or confirmed exposure to participate. An additional 25 participants who have never tested positive for COVID and have not had the vaccine will be enrolled as negative controls. Participants will complete a survey at enrollment. The investigators will also collect blood, nose swab, saliva, stool, semen, and breast milk to test for the virus. The investigators will ask participants to complete a survey and give specimens up to 12 times over 24 months. This information will be used to study how long the virus can live in different parts of the body, antibody development, and post-infectious complications. The investigators hope that this information will allow medical and public health providers to make recommendations to better care for patients in the convalescent phase of COVID-19 infection.

Gender: All

Ages: 7 Years - Any

Updated: 2026-10-05

1 state

COVID-19
Corona Virus Infection
SARS-CoV 2
WITHDRAWN

NCT04361461

Use of Hydroxychloroquine Alone or Associated for Inpatients With SARS-CoV2 Virus (COVID-19)

The Severe Acute Respiratory Syndrome CoronaVirus 2 (SARS-CoV2) has been identified in Wuhan, China, which causes severe pulmonary complications and flu syndrome, which has spread rapidly to all continents. Approximately 25% of hospitalized patients require treatment in intensive care units and 10% require mechanical ventilation. The diagnosis is made by the molecular polymerase chain reaction test. However, diagnostic tests are limited. The clinical care of the patient with COVID-19 is similar to that of patients with severe infectious respiratory complications, consisting of support and oxygen supplementation. Several medications have been tested as remdesivir, a pro-drug nucleoside, which acts by inhibiting viral RNA transcription, although a recently published study has shown no benefit. China recently approved the use of favipiravir, an antiviral used for influenza, as an experimental therapy for COVID-19. Hydroxychloroquine is a drug with great potential treatment, as it can inhibit the pH-dependent steps of replication of various viruses, with a potent effect on SARS-CoV infection and spread. In this way, the present study will evaluate the safety and efficacy of the hydroxychloroquine in patients with symptomatic SARS-Cov2.

Gender: All

Ages: 18 Years - Any

Updated: 2026-09-08

1 state

Coronavirus Infections
SARS-CoV 2
SARS (Severe Acute Respiratory Syndrome)
+1
RECRUITING

NCT07224490

Kisspeptin to Quantify GnRH Neuronal Function in Health and Disease

The objective of this protocol is to use a case-control paradigm to compare the response to an intravenous administration of kisspeptin in individuals with and without post-covid-19 syndrome. The study subjects will receive a single bolus of kisspeptin.

Gender: All

Ages: 18 Years - 60 Years

Updated: 2026-07-13

1 state

Reproductive Disorder
Neurodegeneration
SARS-CoV 2
+1
COMPLETED

NCT04444609

PROSAIC-19 - Prospective Longitudinal Assessment in a COVID-19 Infected Cohort

DESIGN Longitudinal prospective observational multicentre study. Primary objective: Understand the immune mechanisms driving COVID-19 disease in patients with a history of lung disease

Gender: All

Ages: 16 Years - Any

Updated: 2026-07-02

1 state

COVID-19
SARS-CoV 2
ARDS, Human
+1
TERMINATED

NCT04405986

Exploring Brain Damages After COVID-19 Infection

Although direct evidence is currently lacking, the high identity between SARS-CoV-1 and SARS-CoV-2 suggests, that the latter viral strain could also infect the Central Nervous System (CNS). Indeed, some cases of SARS-COV2 encephalitis begin to be described and CNS damages are increasingly highlighted in the literature, but still not objectified by imaging and do not allow to explain the entire clinical patterns. We hypothesise that these CNS damages are not always objectified by Magnetic Resonance Imaging (MRI) but could be indirectly observed by a physiological dysfunction of neural conduction in the brainstem. We will explore brainstem disruption through an electrophysiological approach.

Gender: All

Ages: 18 Years - Any

Updated: 2026-06-09

SARS-CoV 2
ACTIVE NOT RECRUITING

NCT04568148

COVID-19 Biorepository

Establish a COVID-19 biorepository to aid in developing our knowledge of the disease.

Gender: All

Ages: 18 Years - Any

Updated: 2026-05-22

1 state

Covid-19
SARS-CoV 2
Coronavirus
+1
WITHDRAWN

NCT05137795

Inhaled ZYESAMI (Aviptadil Acetate) for Treatment of Severe COVID-19

Brief Summary: SARS-CoV-2 virus infection is known to cause Lung Injury that begins as dyspnea and exercise intolerance, but may rapidly progress to Critical COVID-19 with Respiratory Failure and the need for noninvasive or mechanical ventilation. Mortality rates as high as 80% have been reported among those who require mechanical ventilation, despite best available intensive care. Patients with severe COVID-19 by FDA definition who have not developed respiratory failure be treated with nebulized ZYESAMI™ (aviptadil acetate, a synthetic version of Vasoactive Intestinal Polypeptide (VIP)) 100 μg 3x daily plus Standard of Care vs. placebo + Standard of Care using an FDA 501(k) cleared mesh nebulizer. The primary outcome will be progression in severity of COVID-19 (i.e. critical OR severe progressing to critical) over 28 days. Secondary outcomes will include blood oxygenation as measured by pulse oximetry, dyspnea, exercise tolerance, and levels of TNFα IL-6 and other cytokines.

Gender: All

Ages: 18 Years - 85 Years

Updated: 2026-05-14

SARS-CoV 2
COVID
ARDS
+3
COMPLETED

NCT04359693

Impact of COVID-19 Infection on the Incidence of Ventilator-acquired Infections

Observational cohort study aiming at comparing the incidence of ventilator-associated lower respiratory tract infections between COVID-19 patients and two control groups: one with influenza pneumonia and the other with no viral pneumonia.

Gender: All

Ages: 18 Years - Any

Updated: 2026-04-22

SARS-CoV 2
ACTIVE NOT RECRUITING

NCT04853004

Current and Past SARS-CoV-2 Infection and COVID-19 in Healthcare With Regard to Vaccinations

To investigate the incidence of SARS-CoV-2 infections after vaccination, to monitor the development of SARS-CoV-2 antibody levels after vaccination and to compare this in relation to both previous health \& disease, previous antibody responses and in relation to future disease occurring after vaccination.

Gender: All

Ages: 18 Years - 99 Years

Updated: 2025-03-20

SARS-CoV 2