Gripmax® Nose Child effectiveness in the upper respiratory tract infections treatment

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Abstract

Children are highly predisposed to the respiratory tract infections. Nowadays, attention unit has been focused on the effect of herbal therapy on respiratory tract infections treatment.

Objective. To assess Gripmax® Nose Child effectiveness in patients with rhinitis.

Materials and methods. The open multicentral observational study of safety and effectiveness of the biologically active additive Gripmax® Nose Child. Data collection was performed in various regions of Russia (March–September 2023) via medical records analysis by ambulatory doctors followed by making a special individual registration form. Symptoms were assessed initially (visit 1), after 2–3 days (telephone contact), after 6–7 days (visit 2), after 10–14 days (visit 3). Duration of herbal treatment varied from 7 to 14 days.

Results. Ambulatory medical records of 1073 children aged 3–18 with rhinitis received Gripmax® Nose Child and additional therapy if needed was analyzed. If Gripmax® Nose Child was added to complex therapy, general condition improved, nasal obstruction and secretion significantly reduced from day 2–3. Patients demonstrated statistically significant (p<0,0001) rhinitis symptoms decrease (redness, nasal obstruction and rhinorrhea decrease up to vanishing in 84% by visit 2 and in 99% by visit 3, and up to 96.5% of patients at the treatment course end.

Conclusion. Investigated herbal therapy including herbal components may be recommended as an effective for rhinitis therapy.

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About the authors

N. Geppe

I.M. Sechenov First Moscow State Medical University (Sechenov University), Ministry of Health of Russia

Author for correspondence.
Email: geppe@mail.ru
ORCID iD: 0000-0003-0547-3686

Professor, MD

Russian Federation, Moscow

V. Soboleva

I.M. Sechenov First Moscow State Medical University (Sechenov University), Ministry of Health of Russia; I.I. Mechnikov Research Institute for Vaccines and Sera

Email: geppe@mail.ru
ORCID iD: 0000-0003-1758-5909
Russian Federation, Moscow; Moscow

O. Sukhovjova

I.M. Sechenov First Moscow State Medical University (Sechenov University), Ministry of Health of Russia

Email: geppe@mail.ru
ORCID iD: 0000-0001-5551-7611

Candidate of Medical Sciences

Russian Federation, Moscow

Yu. Isaichkina

I.M. Sechenov First Moscow State Medical University (Sechenov University), Ministry of Health of Russia

Email: geppe@mail.ru
ORCID iD: 0009-0009-7793-1077
Russian Federation, Moscow

M. Tikhonova

Children's City Polyclinic One Hundred and Tenth

Email: geppe@mail.ru
Russian Federation, Moscow

Yu. Alieva

Perm State Medical University named after Academician E. A. Wagner, Ministry of Health of Russia

Email: geppe@mail.ru
ORCID iD: 0000-0002-0283-088X
Russian Federation

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Supplementary files

Supplementary Files
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1. JATS XML
2. Fig. 1. Dynamics of symptoms on the background of therapy (p<0.0001)

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3. Fig. 2. Headache and facial pain severity in patients on the background of treatment

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