Bacteriophage Therapy in Tonsillitis
Primary Purpose
Acute Tonsillitis
Status
Active
Phase
Phase 3
Locations
Uzbekistan
Study Type
Interventional
Intervention
Nebulizer inhalation irrigation of the mucous membranes of the tonsils with a bacteriophage.
Sponsored by
About this trial
This is an interventional supportive care trial for Acute Tonsillitis focused on measuring acute tonsillitis, children, bacteriophage, immunity, ambulatory treatment
Eligibility Criteria
Inclusion Criteria:
- children from 3 to 14 years old.
- children with sore throat.
- children diagnosed with acute tonsillitis.
- children diagnosed with acute respiratory infection (rhinitis, sinusitis, nasopharyngitis).
- children with the opportunity to visit the outpatient clinic.
- children with the ability to receive inhalation therapy.
- children from parents (or guardians) who have given written permission to conduct clinical and laboratory research.
Exclusion Criteria:
- children under 3 years old and over 14 years old.
- children receiving hospital treatment.
- children with acute respiratory tract diseases (bronchitis, pneumonia, pleurisy).
- children with сhronic respiratory tract diseases (bronchitis, pneumonia).
- children who are allergic to antibiotics.
- children with cancer, immunological and hematological diseases.
- children with severe psychological illnesses (schizophrenia, mental retardation, etc.)
- children with cancer, immunological and hematological diseases.
- children with tuberculosis.
Sites / Locations
- Tashkent Pediatric Medical Institute
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Nebulizer inhalation bacteriophage therapy
Arm Description
To study the effects of bacteriophage therapy on acute tonsillitis in children and adolescents in an outpatient setting.
Outcomes
Primary Outcome Measures
Clinical observation of sick children.
Children with clinically diagnosed acute tonsillitis are examined. The clinical study will be carried out on an outpatient basis in cooperation with the clinic of the Tashkent Pediatric Medical Institute. Prior to the study, written permission will be obtained from the parents or guardians of the children to participate in the study. Investigated: anamnesis of the child, the course of the disease, complaints of parents about the child's condition, body temperature in dynamics, visually - the state of the nasopharynx, the manifestation of clinical symptoms (sore throat, headaches, difficulty swallowing food, aphonia, and other signs) in dynamics, the functional state of internal organs (percussion, palpation and auscultation).
Laboratory research methods.
All examined children will undergo general clinical examination and pharyngoscopy. Additionally, all patients will have tonsil swabs for bacteriological examination (bacteriological culture, n x 10⁴/mL ) according to the standard technique. Also, swabs from the nasopharynx will be taken for viral lesions by the standard method - PCR (polymerase chain reaction). The research will be carried out in specialized laboratories.
Experimental clinical stage. Bacteriophage therapy.
Comprehensive outpatient treatment will be based on standard clinical guidelines. Patients will be prescribed antibiotic therapy based on possible pathogens. Patients will receive bacteriophage therapy using a liquid pyobacteriophage complex (liquid pyobacteriophage complex - PCL), through nebulizer inhalation to irrigate the mucous membranes of the tonsils. Just 5 ml PCL for 10 minutes once every 5 days. Efficacy will be studied based on immunological studies.A study of cellular (class of T-lymphocytes, Inflammatory cytokines (e.g., IL-1,2,4,5,6,11,13 - U/ml) and TNF-α) and humoral ( IgA / IgM / IgG -IU/mL) immunity in children will be carried out, using (Enzyme Linked Immunosorbent Assay) ELISA which is an immunoassay, suited to the determination of antibodies in the field of infectious serology.
Secondary Outcome Measures
The second stage of the study (statistical).
The results will be analyzed using a statistical program based on Excel 2017 (Microsoft Office 2017). Clinical signs will be calculated as a percentage (%) incidence. We will calculate the chi-square (χ2) test or Fisher's exact test (for expected values <5) to assess if certain pairs of microbes are more common than expected by chance in bacteriological examination. In addition, we will use the Kruskal-Wallis test to compare the average delay between disease onset and sample collection between samples containing one or more organisms. When evaluating immunological analyzes, characterizing the statistical significance of differences, the Student's t-test will be used with the definition of the confidence interval. The X-square test will be used to assess the frequency of identifying qualitative features. In all analyzes, P ≤ 0.05 was considered significant.
Full Information
NCT ID
NCT04682964
First Posted
December 9, 2020
Last Updated
October 21, 2022
Sponsor
Tashkent Pediatric Medical Institute
1. Study Identification
Unique Protocol Identification Number
NCT04682964
Brief Title
Bacteriophage Therapy in Tonsillitis
Official Title
Bacteriophage Therapy in Acute Tonsillitis
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 2, 2020 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tashkent Pediatric Medical Institute
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The patients received bacteriophage therapy with a liquid piobacteriophage complex (liquid pyobacteriophage complex - PCL). PСL was administered via nebulizer inhalation to irrigate the tonsil mucosa. A total of 5 ml of PCL was inhaled for 10 minutes every 5 days. The drug causes the lysis of certain bacteria, including staphylococcus, enterococcus, streptococcus, enteropathogenic E. coli, Proteus vulgaris, Proteus mirabilis, Pseudomonas aeruginosa, Klebsiella pneumoniae and Klebsiella oxytoca. The choice of this drug was based on bacteriological studies.
Detailed Description
Comprehensive outpatient treatment was based on standard clinical guidelines, and symptomatic treatment was performed. On the first day of diagnosis, patients were prescribed complex antibacterial therapy on the basis of possible causative agents. Subsequently, antibiotic therapy was adjusted based on the results of the bacteriological examinations. A total of 67 patients received bacteriophage therapy using a liquid complex of pyobacteriophages (pyobacteriophage complex liquid - PСL). PСL was administered via nebulizer inhalation to irrigate the mucous membranes of the tonsils. In total, 5 ml of PCL was inhaled for up to 10 minutes once every 5 days.
The drug causes lysis of specific bacteria including Staphylococcus, Enterococcus, Streptococcus, enteropathogenic Escherichia coli, Proteus vulgaris, Proteus mirabilis, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Klebsiella oxytoca. The drug is recommended for use for diseases of the ear, throat, nose, respiratory tract and lungs; inflammation of the sinuses and middle ear; tonsillitis; pharyngitis; laryngitis; tracheitis; bronchitis; pneumonia, pleurisy; and other inflammatory diseases. The choice of this drug was based on bacteriological studies.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Tonsillitis
Keywords
acute tonsillitis, children, bacteriophage, immunity, ambulatory treatment
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Model Description
Children aged 3 to 14 years with clinically diagnosed acute tonsillitis will receive bacteriophage therapy using a liquid pyobacteriophage complex (liquid pyobacteriophage complex - PCL).
Masking
None (Open Label)
Allocation
N/A
Enrollment
128 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Nebulizer inhalation bacteriophage therapy
Arm Type
Experimental
Arm Description
To study the effects of bacteriophage therapy on acute tonsillitis in children and adolescents in an outpatient setting.
Intervention Type
Drug
Intervention Name(s)
Nebulizer inhalation irrigation of the mucous membranes of the tonsils with a bacteriophage.
Other Intervention Name(s)
Bacteriophage therapy.
Intervention Description
Bacteriophage therapy using a liquid complex of pyobacteriophages (pyobacteriophage complex liquid - PСL). PСL was administered via nebulizer inhalation to irrigate the mucous membranes of the tonsils. In total, 5 ml of PCL was inhaled for up to 10 minutes once every 5 days.
Primary Outcome Measure Information:
Title
Clinical observation of sick children.
Description
Children with clinically diagnosed acute tonsillitis are examined. The clinical study will be carried out on an outpatient basis in cooperation with the clinic of the Tashkent Pediatric Medical Institute. Prior to the study, written permission will be obtained from the parents or guardians of the children to participate in the study. Investigated: anamnesis of the child, the course of the disease, complaints of parents about the child's condition, body temperature in dynamics, visually - the state of the nasopharynx, the manifestation of clinical symptoms (sore throat, headaches, difficulty swallowing food, aphonia, and other signs) in dynamics, the functional state of internal organs (percussion, palpation and auscultation).
Time Frame
study of one patient - 4 weeks
Title
Laboratory research methods.
Description
All examined children will undergo general clinical examination and pharyngoscopy. Additionally, all patients will have tonsil swabs for bacteriological examination (bacteriological culture, n x 10⁴/mL ) according to the standard technique. Also, swabs from the nasopharynx will be taken for viral lesions by the standard method - PCR (polymerase chain reaction). The research will be carried out in specialized laboratories.
Time Frame
study of one patient - 2 weeks
Title
Experimental clinical stage. Bacteriophage therapy.
Description
Comprehensive outpatient treatment will be based on standard clinical guidelines. Patients will be prescribed antibiotic therapy based on possible pathogens. Patients will receive bacteriophage therapy using a liquid pyobacteriophage complex (liquid pyobacteriophage complex - PCL), through nebulizer inhalation to irrigate the mucous membranes of the tonsils. Just 5 ml PCL for 10 minutes once every 5 days. Efficacy will be studied based on immunological studies.A study of cellular (class of T-lymphocytes, Inflammatory cytokines (e.g., IL-1,2,4,5,6,11,13 - U/ml) and TNF-α) and humoral ( IgA / IgM / IgG -IU/mL) immunity in children will be carried out, using (Enzyme Linked Immunosorbent Assay) ELISA which is an immunoassay, suited to the determination of antibodies in the field of infectious serology.
Time Frame
study of one patient - 4 weeks
Secondary Outcome Measure Information:
Title
The second stage of the study (statistical).
Description
The results will be analyzed using a statistical program based on Excel 2017 (Microsoft Office 2017). Clinical signs will be calculated as a percentage (%) incidence. We will calculate the chi-square (χ2) test or Fisher's exact test (for expected values <5) to assess if certain pairs of microbes are more common than expected by chance in bacteriological examination. In addition, we will use the Kruskal-Wallis test to compare the average delay between disease onset and sample collection between samples containing one or more organisms. When evaluating immunological analyzes, characterizing the statistical significance of differences, the Student's t-test will be used with the definition of the confidence interval. The X-square test will be used to assess the frequency of identifying qualitative features. In all analyzes, P ≤ 0.05 was considered significant.
Time Frame
4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
children from 3 to 14 years old.
children with sore throat.
children diagnosed with acute tonsillitis.
children diagnosed with acute respiratory infection (rhinitis, sinusitis, nasopharyngitis).
children with the opportunity to visit the outpatient clinic.
children with the ability to receive inhalation therapy.
children from parents (or guardians) who have given written permission to conduct clinical and laboratory research.
Exclusion Criteria:
children under 3 years old and over 14 years old.
children receiving hospital treatment.
children with acute respiratory tract diseases (bronchitis, pneumonia, pleurisy).
children with сhronic respiratory tract diseases (bronchitis, pneumonia).
children who are allergic to antibiotics.
children with cancer, immunological and hematological diseases.
children with severe psychological illnesses (schizophrenia, mental retardation, etc.)
children with cancer, immunological and hematological diseases.
children with tuberculosis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shokhida T. Turdieva, MD
Organizational Affiliation
Tashkent Pediatric Medical Institute
Official's Role
Study Director
Facility Information:
Facility Name
Tashkent Pediatric Medical Institute
City
Tashkent
ZIP/Postal Code
100140
Country
Uzbekistan
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
We are planning to create a joint project to research the treatment of bacterial infection in children with respiratory diseases by COVED-19.
IPD Sharing Time Frame
2021-2024
IPD Sharing Access Criteria
Children 0-17 years old, after being diagnosed with COVID-19, with a bacterial infection of the upper respiratory tract. We will work together with children's hospitals and research centers.
Learn more about this trial
Bacteriophage Therapy in Tonsillitis
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