Treatment of Allergic Rhinitis and Chronic Polypous Rhinosinusitis With Olfactory Mucosa-derived Mesenchymal Stem Cells

Sponsor
Institute of Biophysics and Cell Engineering of National Academy of Sciences of Belarus (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05167552
Collaborator
The Republican Center for Research and Practice in Otolaryngology (Other)
60
4
22

Study Details

Study Description

Brief Summary

Treatment of patients with allergic rhinitis and chronic polypous rhinosinusitis with olfactory mucosa-derived mesenchymal stem cells

Condition or Disease Intervention/Treatment Phase
  • Biological: Olfactory mucosa-derived mesenchymal stem cells
  • Other: Standard treatment of type Allergic Rhinitis according to the clinical protocols
  • Other: Standard treatment of type Chronic Polypous Rhinosinusitis according to the clinical protocols
Phase 1/Phase 2

Detailed Description

During the implementation of the project, the methods for the treatment of allergic rhinitis and chronic polypous rhinosinusitis with olfactory mucosa-derived mesenchymal stem cells will be developed.

The positive outlook for the effectiveness of MSCs is due to the following:
  • knowledge of the leading role of immunopathogenetic mechanisms in the development of allergic rhinitis and chronic polypous rhinosinusitis and the pronounced immunomodulating properties of MSCs;

  • the ability of MSCs to reduce the production of proinflammatory cytokines and suppress immune inflammation;

  • positive results of preclinical studies of the method of treatment of diseases accompanied by over-activation of the immune system, including autoimmune diseases, in animals and the first clinical studies in patients.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Treatment of Patients With Allergic Rhinitis and Chronic Polypous Rhinosinusitis With Olfactory Mucosa-derived Mesenchymal Stem Cells
Anticipated Study Start Date :
Mar 1, 2022
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Patients with allergic rhinitis receiving standard treatment and mesenchymal stem cells

Group 1: Patients with allergic rhinitis receiving standard treatment and olfactory mucosa-derived mesenchymal stem cells

Biological: Olfactory mucosa-derived mesenchymal stem cells
Olfactory mucosa-derived mesenchymal stem cells

Other: Standard treatment of type Allergic Rhinitis according to the clinical protocols
Standard treatment of type Allergic Rhinitis according to the clinical protocols

Experimental: Patients with chronic rhinosinusitis receiving standard treatment and mesenchymal stem cells

Group 2: Patients with chronic polypous rhinosinusitis receiving standard treatment and olfactory mucosa-derived mesenchymal stem cells

Biological: Olfactory mucosa-derived mesenchymal stem cells
Olfactory mucosa-derived mesenchymal stem cells

Other: Standard treatment of type Chronic Polypous Rhinosinusitis according to the clinical protocols
Standard treatment of type Chronic Polypous Rhinosinusitis according to the clinical protocols

Active Comparator: Patients with allergic rhinitis receiving standard treatment

Group 3: Patients with allergic rhinitis receiving standard treatment

Other: Standard treatment of type Allergic Rhinitis according to the clinical protocols
Standard treatment of type Allergic Rhinitis according to the clinical protocols

Active Comparator: Patients with chronic polypous rhinosinusitis receiving standard treatment

Group 4: Patients with chronic polypous rhinosinusitis receiving standard treatment

Other: Standard treatment of type Chronic Polypous Rhinosinusitis according to the clinical protocols
Standard treatment of type Chronic Polypous Rhinosinusitis according to the clinical protocols

Outcome Measures

Primary Outcome Measures

  1. The relapse-free period [6 month]

    The duration of the relapse-free period

  2. The relapse-free period [1 year]

    The duration of the relapse-free period

  3. The need for surgical intervention [1 year]

    The need for surgical intervention

  4. The need for the use of basic drug therapy [6 month]

    The need for the use of basic drug therapy

  5. The need for the use of basic drug therapy [1 year]

    The need for the use of basic drug therapy

  6. Adverse effects associated with the therapy [1 month]

    Determination of adverse effects associated with the therapy

  7. Adverse effects associated with the therapy [1 year]

    Determination of adverse effects associated with the therapy

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Clinical diagnosis of allergic rhinitis or chronic polyposis rhinosinusitis

  • The patient can read, understand, follow the examination procedures and complete, if necessary, the required documentation

  • Written informed consent

Exclusion Criteria:
  • The presence of any malignant tumor within the last 5 years

  • Acute or chronic diseases in the stage of decompensation

  • Chronic infectious diseases: HIV, viral hepatitis B, C, tuberculosis

  • Patients who are pregnant, breastfeeding, or fertile patients who are not using adequate contraceptive methods

  • Chronic and protracted mental disorders, all diseases with the presence of the syndrome of dependence on alcohol, drugs and psychoactive substances, any other condition that makes the patient unable to understand the nature, extent and possible consequences of the study or, in the opinion of the researcher, prevents the patient from observing and performing protocol

  • Patients are unable or unwilling to give written informed consent and / or follow research procedures

  • Any other medical condition that, in the opinion of the investigator, may be associated with an increased risk to the patient or may affect the outcome or evaluation of the study

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Institute of Biophysics and Cell Engineering of National Academy of Sciences of Belarus
  • The Republican Center for Research and Practice in Otolaryngology

Investigators

  • Study Director: Natalia Antonevich, Dr, the Institute of Biophysics and Cell Engineering of National Academy of Sciences of Belarus
  • Study Director: Yulia Eremenko, Prof, The Republican Center for Research and Practice in Otolaryngology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Institute of Biophysics and Cell Engineering of National Academy of Sciences of Belarus
ClinicalTrials.gov Identifier:
NCT05167552
Other Study ID Numbers:
  • IBCE_AllRhin
First Posted:
Dec 22, 2021
Last Update Posted:
Jan 19, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 19, 2022