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Impact of Nasal Saline Irrigations on Viral Load in Patients With COVID-19

Primary Purpose

COVID 19

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Saline Nasal Irrigation
Saline with Baby Shampoo Nasal Irrigation
Sponsored by
Vanderbilt University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID 19

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients testing positive for COVID-19 at Vanderbilt University Medical Center or VUMC-associated testing centers
  • Age of 18 years or greater
  • Patients must be planning self-quarantine after infection in the greater Nashville area within a 30-mile radius of Vanderbilt University Medical Center

Exclusion Criteria:

  • Requiring hospitalization - only outpatient COVID-19 cases are eligible for the study
  • Current use of nasal saline irrigations or other intranasal medications
  • Inability to perform saline irrigations/nasal swabs in separate bathroom away from household contacts

Sites / Locations

  • Vanderblt University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Control Group, No intervention

Saline Nasal Irrigation

Saline with Baby Shampoo Nasal Irrigation

Arm Description

control group, no nasal irrigation

Nasal irrigation BID with normal saline

Nasal irrigation BID with normal saline and 1/2 teaspoon baby shampoo

Outcomes

Primary Outcome Measures

Change in SARS-CoV-2 mucosal immune response in the nasopharynx
Viral RNA will be extracted using a standard Qiagen viral RNA isolation kit. An established, high-throughput CoV genome sequencing pipeline will be used to perform overlapping long-range RT-PCR across the viral genome for each viral genome proposed in this project.
Change in microbial load in the nasopharynx
Evaluate microbial sequence data in the context of SARS-CoV-2 infection status to determine taxonomic profiles and their distributions within and between samples.
Change in Viral Load in the nasopharynx over the course of COVID-19 infection
Perform qPCR Analysis to asses viral copy number.

Secondary Outcome Measures

Symptom assessment
Identify symptom burden during the course of the disease via self-report
Temperature assessment
Identify temperature during the course of the disease via self-report

Full Information

First Posted
April 11, 2020
Last Updated
May 16, 2022
Sponsor
Vanderbilt University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04347538
Brief Title
Impact of Nasal Saline Irrigations on Viral Load in Patients With COVID-19
Official Title
Impact of Nasal Saline Irrigations on Viral Load in Patients With COVID-19
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
May 1, 2020 (Actual)
Primary Completion Date
March 16, 2022 (Actual)
Study Completion Date
March 16, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Nasal saline irrigations are a safe and commonly used mechanism to treat a variety of sinonasal diseases including sinusitis, rhinitis, and upper respiratory tract infections. When used properly, these irrigations are a safe and easy intervention available over the counter without a prescription. Additionally, baby shampoo has been found to be a safe additive functioning as a surfactant when a small amount is added to the saline rinses which may help augment clearance of the sinonasal cavity. While many systemic medications and treatments have been proposed for COVID-19, there has not yet been a study looking at targeted local intervention to the nasal cavity and nasopharynx where the viral load is the highest. Studies have shown that the use of simple over the counter nasal saline irrigations can decrease viral shedding in the setting of viral URIs, including the common coronavirus (not SARS-CoV-2). Further, as SARS-CoV-2 is an enveloped virus, mild-detergent application with nasal saline would neutralize the virus further. It is our hypothesis that nasal saline or nasal saline with baby shampoo irrigations may decrease viral shedding/viral load and viral transmission, secondary bacterial load, nasopharyngeal inflammation in patients infected with the novel SARS-CoV-2.
Detailed Description
The novel coronavirus known as SARS-CoV-2 and the associated disease process COVID-19 (coronavirus disease 2019) was first seen in late 2019 in Wuhan, China. Over the following months, it quickly spread across the continent and, in short order, the globe, making an impact that hasn't been seen in generations. Although coronaviruses have been prevalent for millennia, this version is immunologically novel, and thus there is no natural immunity to the virus. This has been a major reason for its rapid spread across the world. Previous members of the coronavirus family have typically caused upper respiratory symptoms such as the common cold, though there have also been more virulent versions of this virus seen in the recent past, such as SARS (Severe Acute Respiratory Syndrome) and MERS (Middle East Respiratory Syndrome). Similarly named, SARS-CoV-2 also causes upper respiratory symptoms but has varied from the previous viral syndromes in a number of ways including how quickly it has been able to transmit within a population. This is a disease that does not segregate and can affect all ages, genders, and ethnicities. Everyone is susceptible to this virus. New diagnostic and therapeutic approaches for respiratory viruses are also being rapidly developed and polymerase chain reaction-based (PCR) diagnostics and multiplex assays are increasingly used in clinical laboratories for SARS-CoV-2 clinical detection and subtyping. Rapid antigenic and genetic evolution has been expected for SARS-CoV-2 strains, and a better understanding of SARS-CoV-2 evolutionary dynamics is needed to establish an effective vaccine. Our present understanding of the nature and extent of the upper respiratory track (URT) microbiome in humans is limited. Furthermore, we have little understanding of how acute viral respiratory infections of SARS-CoV-2 influence the URT microbiome, or how genotypic differences in the virus influence the URT microbiome and vice versa. Innate immune responses to pathogens, along with dysregulation of inflammation, are key factors involved in pathogenesis, and different viral pathogens activate different types of inflammatory responses. Respiratory viral infection i.e., SARS-CoV-2 infection is expected to activate TLR2, TLR3, TLR4 and TLR7 responses and this is likely to modulate commensal microbiota populations. It is not yet known if the severity of SARS-CoV-2 disease in older adults is due to a biased host response, SARS-CoV-2 virulence determinants, or the impact infection has on commensal microbiota. Up to this point, there is no unanimously approved treatment for the disease nor is there a vaccine or antiviral drugs available for the public. The primary methods for treatment of this deadly virus have been supportive in nature including intubation in severe cases with respiratory failure. While a unanimous treatment has yet to be discovered, there has been a great amount of knowledge garnered over the last few months about the virus and the disease that accompanies it. Several studies have demonstrated high viral titers within the nasopharynx and oral cavity and many have posited that this is the primary source of infection and viral replication. Additionally, a high nasal/nasopharyngeal viral load has been associated with increased symptoms and higher severity of the disease. Interestingly, there have been a number of studies recently looking at the effect of nasal saline irrigations in the setting of viral URIs, including coronaviruses (not including SARS-CoV-2). One of the major takeaways from these studies was decreased viral shedding in patients treated with saline irrigations compared to the control group. Nasal saline irrigations are available over the counter and widely viewed as both safe and affordable. Could these irrigations have a similar effect on the novel SARS-CoV-2 that they have on other viral respiratory infections?

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID 19

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients enrolled will be randomized to one of three treatment groups (1. control- no intervention, 2. intervention 1 - nasal saline irrigations BID, 3. intervention 2- nasal saline irrigations with ½ teaspoon surfactant (Johnson's baby shampoo) BID).
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control Group, No intervention
Arm Type
No Intervention
Arm Description
control group, no nasal irrigation
Arm Title
Saline Nasal Irrigation
Arm Type
Experimental
Arm Description
Nasal irrigation BID with normal saline
Arm Title
Saline with Baby Shampoo Nasal Irrigation
Arm Type
Experimental
Arm Description
Nasal irrigation BID with normal saline and 1/2 teaspoon baby shampoo
Intervention Type
Other
Intervention Name(s)
Saline Nasal Irrigation
Intervention Description
Saline nasal irrigation BID
Intervention Type
Other
Intervention Name(s)
Saline with Baby Shampoo Nasal Irrigation
Intervention Description
Saline with 1/2 teaspoon Baby Shampoo Nasal Irrigation.
Primary Outcome Measure Information:
Title
Change in SARS-CoV-2 mucosal immune response in the nasopharynx
Description
Viral RNA will be extracted using a standard Qiagen viral RNA isolation kit. An established, high-throughput CoV genome sequencing pipeline will be used to perform overlapping long-range RT-PCR across the viral genome for each viral genome proposed in this project.
Time Frame
Day 1 to day 21
Title
Change in microbial load in the nasopharynx
Description
Evaluate microbial sequence data in the context of SARS-CoV-2 infection status to determine taxonomic profiles and their distributions within and between samples.
Time Frame
Day 1 to day 21
Title
Change in Viral Load in the nasopharynx over the course of COVID-19 infection
Description
Perform qPCR Analysis to asses viral copy number.
Time Frame
Day 1 to day 21
Secondary Outcome Measure Information:
Title
Symptom assessment
Description
Identify symptom burden during the course of the disease via self-report
Time Frame
21 days
Title
Temperature assessment
Description
Identify temperature during the course of the disease via self-report
Time Frame
21 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients testing positive for COVID-19 at Vanderbilt University Medical Center or VUMC-associated testing centers Age of 18 years or greater Patients must be planning self-quarantine after infection in the greater Nashville area within a 30-mile radius of Vanderbilt University Medical Center Exclusion Criteria: Requiring hospitalization - only outpatient COVID-19 cases are eligible for the study Current use of nasal saline irrigations or other intranasal medications Inability to perform saline irrigations/nasal swabs in separate bathroom away from household contacts
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kyle Kimura, MD
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Justin H. Turner, MD, PhD
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Study Director
Facility Information:
Facility Name
Vanderblt University Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35040594
Citation
Esther CR Jr, Kimura KS, Mikami Y, Edwards CE, Das SR, Freeman MH, Strickland BA, Brown HM, Wessinger BC, Gupta VC, Von Wahlde K, Sheng Q, Huang LC, Bacon DR, Kimple AJ, Ceppe AS, Kato T, Pickles RJ, Randell SH, Baric RS, Turner JH, Boucher RC. Pharmacokinetic-based failure of a detergent virucidal for severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) nasal infections: A preclinical study and randomized controlled trial. Int Forum Allergy Rhinol. 2022 Sep;12(9):1137-1147. doi: 10.1002/alr.22975. Epub 2022 Jan 31.
Results Reference
derived

Learn more about this trial

Impact of Nasal Saline Irrigations on Viral Load in Patients With COVID-19

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