Page last updated: 2024-10-24

cetylpyridinium and Catarrh

cetylpyridinium has been researched along with Catarrh in 2 studies

Cetylpyridinium: Cationic bactericidal surfactant used as a topical antiseptic for skin, wounds, mucous membranes, instruments, etc.; and also as a component in mouthwash and lozenges.

Catarrh: Inflammation of a mucous membrane with increased flow of mucous in humans or animals. Catarrh is used mostly in a historical context.

Research Excerpts

ExcerptRelevanceReference
"Prior influenza vaccination had no effect on study outcome."2.84Randomized, double-blind, placebo-controlled clinical trial to assess the safety and effectiveness of a novel dual-action oral topical formulation against upper respiratory infections. ( Adkins, I; Arters, K; Buchheit, K; Esper, F; Ghannoum, MA; Mukherjee, PK; Salata, RA, 2017)
"Whether the absence rate due to common cold and influenza changed by encouraging the use of the PVP-I gargle was determined by comparing a middle school where the PVP-I gargle was used and other middle schools where it was not."1.31Evaluation of the bactericidal activity of povidone-iodine and commercially available gargle preparations. ( Nakagawa, Y; Shiraishi, T, 2002)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mukherjee, PK1
Esper, F1
Buchheit, K1
Arters, K1
Adkins, I1
Ghannoum, MA1
Salata, RA1
Shiraishi, T1
Nakagawa, Y1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Pilot Study of the Safety, Tolerability, and Effectiveness of Halo to Prevent Acute Upper Respiratory Disease and Respiratory Virus Infections[NCT02644135]100 participants (Actual)Interventional2013-01-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Number of Acute Respiratory Illnesses

Measured by medical record review. (NCT02644135)
Timeframe: Through study duration, an average of 3 months

InterventionNumber of acute respiratory illnesses (Number)
Halo Oral Spray4
Halo Placebo2

Number of Participants That Develop Acute Respiratory Illnesses When Using Halo vs Placebo

(NCT02644135)
Timeframe: Through study duration, an average of 3 months

Interventionparticipants (Number)
Halo Oral Spray2
Halo Placebo4

Trials

1 trial available for cetylpyridinium and Catarrh

ArticleYear
Randomized, double-blind, placebo-controlled clinical trial to assess the safety and effectiveness of a novel dual-action oral topical formulation against upper respiratory infections.
    BMC infectious diseases, 2017, 01-14, Volume: 17, Issue:1

    Topics: Administration, Oral; Administration, Topical; Adolescent; Adult; Anti-Infective Agents, Local; Cety

2017

Other Studies

1 other study available for cetylpyridinium and Catarrh

ArticleYear
Evaluation of the bactericidal activity of povidone-iodine and commercially available gargle preparations.
    Dermatology (Basel, Switzerland), 2002, Volume: 204 Suppl 1

    Topics: Adolescent; Adult; Anti-Infective Agents, Local; Cetylpyridinium; Common Cold; Humans; Influenza, Hu

2002