Pregled bibliografske jedinice broj: 1170277
Safety and Efficacy Assessment of Stérimar Stop and Protect Cold for Adults and Stérimar Blocked Nose in Common Cold: A Randomized, Double-blind, Controlled Parallel-group, Clinical Study
Safety and Efficacy Assessment of Stérimar Stop and Protect Cold for Adults and Stérimar Blocked Nose in Common Cold: A Randomized, Double-blind, Controlled Parallel-group, Clinical Study // Acta Scientific Otolaryngology, 4 (2022), 1; 7-17 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1170277 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Safety and Efficacy Assessment of Stérimar Stop and Protect Cold for Adults and Stérimar Blocked
Nose in Common Cold: A Randomized, Double-blind, Controlled Parallel-group, Clinical Study
Autori
Sbrocca, Federica ; Saaid, Amina ; Culig, Josip
Izvornik
Acta Scientific Otolaryngology (2582-5550) 4
(2022), 1;
7-17
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Nasal Irrigation ; Common Cold ; Hypertonic Solutions ; Seawater ; Hyaluronic Acid ; Copper
Sažetak
Background: Current treatment options for common cold focus on symptomatic relief. Nasal irrigation is a safe, inexpensive and effective adjunct treatment to reduce common cold-associated nasal congestion ; it also improves quality of life and decreases medication use. Purpose: The objective of this work was to investigate safety and efficacy of a novel microfiltered hypertonic seawater solution enriched with hyaluronic acids, eucalyptus oil and copper salts (SSPCA) on relieving common cold symptoms in comparison to a hypertonic seawater solution enriched with copper salts only (SBN). Methods: In total, 102 common cold patients were randomized to use SSPCA (n = 51) or SBN (n = 51) until their common cold episode was resolved (maximum 14 days). Illness severity evaluated by means of the validated 21-item Wisconsin Upper Respiratory Symptom Survey (WURSS-21) was the primary endpoint. Illness duration, use of rescue medication, patient satisfaction and acceptability were secondary endpoints measured through patient diaries. In addition, nasal presence of 24 airway pathogens was screened via RT-PCR before and after treatment. Results: Based on subjective patient diaries, SSPCA was as effective as SBN in reducing overall illness/symptom severity, improving quality of life and satisfying patient expectations. SSPCA had a faster onset of action than SBN in nasal decongestion (p = 0.0056), symptom and breathing relief (p = 0.0028 and p = 0.0128, respectively), stopping cold symptoms (p = 0.0002), and improving nasal well-being (p = 0.0279). Amount of airway pathogens - including rhino- and adenoviruses - was significantly lower after the treatment compared to pre-treatment, with no difference between groups. No adverse events were reported. Conclusion: Both SSPCA and SBN appear to be safe and effective solutions that enable symptomatic relief and decrease the presence of nasal viruses in common cold patients. However, SSPCA had a faster onset of action compared to SBN in nasal decongestion and breathing relief, improving common cold symptoms and nasal well-being.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Zdravstveno veleučilište, Zagreb,
Veleučilište Velika Gorica
Profili:
Josip Čulig
(autor)
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