Mucosal Immunity: Influence on Infectious Viral Load: a Prospective Observational Study
NCT05794412 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 320
Last updated 2025-01-14
Summary
The goal of this observational study is to learn about the influence of pre-existing mucosal immunity, i.e. antibodies and immune cells that are present at the nasal mucosa before infection, on the infectious viral load after infection with SARS-CoV-2, influenza virus and RSV. The investigators will include app. 320 participants which will be followed for up to 17 months. During this time, the investigators will monitor their nasal mucosal antibodies at regular intervals and compare them to their infectious viral load if they are infected with SARS-CoV-2, influenza virus or RSV. Participants are invited to take a test for SARS-CoV-2, influenza virus or RSV in case of respiratory symptoms. If participants are positive the investigators will follow their viral load kinetics by taking nasopharyngeal swabs every 2-3 days. The investigators will also record the duration and strength of the following symptoms:
* Cough
* Fever
* Tired
* Sore throat
* Difficulty breathing
* Respiratory distress
* Headache
* Loss (or alteration) of smell
* Loss (or alteration) of sense of taste
* Myalgias
* Chills
* Subjective fever
* Pink sputum (or coughing up blood)
* Thoracic pain
* Runny nose
* Abdominal pain
* Nausea
* Vomiting
* Diarrhea
* Constipation
* Irritated or watery eyes
* Rashes
* Other
Conditions
- SARS-CoV-2 Infection
- Influenza Viral Infections
- Virus Shedding
- Mucosal Immunity
- RSV Infection
Interventions
- OTHER
-
No intervention
No intervention
Sponsors & Collaborators
-
University of Geneva, Switzerland
collaborator OTHER -
ModernaTX, Inc.
collaborator INDUSTRY -
University Hospital, Geneva
lead OTHER
Principal Investigators
-
Benjamin Meyer, Dr. · University of Geneva
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-01-10
- Primary Completion
- 2024-12-31
- Completion
- 2024-12-31
Countries
- Switzerland
Study Locations
More Related Trials
-
Study of the Use of Nasal IFN-γ in Patients for the Prevention of Acute Respiratory Viral Infections, Icluding COVID-19
NCT05054114 ·Status: COMPLETED ·Phase: NA
-
The Safety and Tolerability of MY-586 COVID-19 Neutralizing Antibody Nasal Spray in Healthy Subjects
NCT05977101 ·Status: UNKNOWN ·Phase: NA
-
A Phase I, Randomized, Double-Blind, Single-Dose, Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of MEDI-557
NCT00578682 ·Status: COMPLETED ·Phase: PHASE1
-
SARS-CoV-2 Immune Responses After COVID-19 Therapy and Subsequent Vaccine
NCT04952402 ·Status: COMPLETED ·Phase: PHASE4
-
Characterization and Durability of COVID-19 Vaccine Induced Immune Responses in Healthcare/Frontline Workers
NCT05049187 ·Status: COMPLETED
-
Study to Evaluate the Human Infection of the Lower Respiratory Tract in Children at High Risk
NCT00192439 ·Status: COMPLETED
-
RI-001 in Immunosuppressed Respiratory Syncytial Virus (RSV) Infected Patients at Risk of Lower Tract RSV Illness
NCT00632463 ·Status: COMPLETED ·Phase: PHASE2
-
A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety of MEDI-559 in Healthy 1 to <24 Month-Old Children
NCT00767416 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Intranasal Challenge of Healthy Adults With Respiratory Syncytial Virus (RSV)
NCT01475305 ·Status: TERMINATED ·Phase: PHASE1
-
Safety, Tolerability, and Pharmacokinetics of RSV Monoclonal Antibody RSM01 in Healthy Adults
NCT05118386 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Safety, Tolerability, Immunogenicity and Vaccine-like Viral Shedding of MEDI-534, Against Respiratory Syncytial Virus (RSV) and Parainfluenza Virus Type 3 (PIV3), in Healthy 6 to <24 Month-old Children and in 2 Month-old Infants
NCT00686075 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Study to Evaluate the Safety and Ability of the Vaccine to Induce Antibodies Against the Respiratory Syncytial Virus in Healthy Adults
NCT02298179 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Safety, Tolerability, and Immunogenicity of MVC-COV1901 or MVC-COV1901(Beta) Against COVID-19
NCT05216601 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Immunogenicity of an Intranasal RSV Vaccine Expressing SARS-CoV-2 Spike Protein (COVID-19 Vaccine) in Adults
NCT04798001 ·Status: UNKNOWN ·Phase: PHASE1
-
COVID-19 Vaccine Induced Adaptive Immune Responses
NCT04729374 ·Status: UNKNOWN
-
A Phase 1 Study to Evaluate the Pharmacokinetics, Metabolism, and Excretion of GS-5806
NCT01801293 ·Status: COMPLETED ·Phase: PHASE1
-
Study Understanding Pre-Exposure pRophylaxis of NOVel Antibodies (SUPERNOVA) Sub-study: Study Understanding Pre-Exposure pRophylaxis of NOVel Antibodies (SUPERNOVA) Sub-study
NCT05648110 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Safety and Immunogenicity of the RSV D46cpΔM2-2 Vaccine in RSV-Seropositive Children and RSV-Seronegative Infants and Children
NCT02601612 ·Status: COMPLETED ·Phase: PHASE1
-
MEDI-557 Adult Dosing
NCT01562938 ·Status: COMPLETED ·Phase: PHASE1
-
Presatovir in Hematopoietic Cell Transplant Recipients With Respiratory Syncytial Virus (RSV) Infection of the Lower Respiratory Tract
NCT02254421 ·Status: COMPLETED ·Phase: PHASE2
-
A Study on the Safety and Immune Response to an mRNA-based RSV Investigational Vaccine in Healthy Adults Aged 18-45 Years
NCT06573281 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1
-
Study Will Assess the Safety, Neutralizing Activity and Efficacy of AZD3152 in Adults With Conditions Increasing Risk of Inadequate Protective Immune Response After Vaccination and Thus Are at High Risk of Developing Severe COVID-19
NCT06057064 ·Status: COMPLETED ·Phase: PHASE2
-
Factors Influencing the COVID-19 Vaccine Immune Response According to Age and Presence or Not of a Past History of COVID-19
NCT05047718 ·Status: COMPLETED ·Phase: PHASE4
-
RSV Challenge in Healthy Adults
NCT00100373 ·Status: COMPLETED ·Phase: NA
-
Study of Immune Response in Subjects Vaccinated Against SARS-CoV-2 Infection
NCT07049497 ·Status: COMPLETED