Higher Versus Standard Dose of Amoxicillin-clavulanate in Pediatric PBB
Primary Purpose
Protracted Bacterial Bronchitis
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Amoxicillin-Clavulanate 200 Mg-28.5 Mg Oral dry suspension
Sponsored by
About this trial
This is an interventional treatment trial for Protracted Bacterial Bronchitis
Eligibility Criteria
Inclusion Criteria:
- Children diagnosed with first-onset PBB
- Subjects and their guardians agree to participate in the study and sign an informed consent
Exclusion Criteria:
- Seriously delayed development of the nervous system;
- With severe underlying diseases: such as severe neuromuscular diseases, immunodeficiency, malnutrition, heart diseases, congenital respiratory system malformation, and other diseases of the heart, brain, liver, kidney and blood system;
- Other diseases that can cause chronic wet cough, including chronic rhinitis, sinusitis, interstitial lung disease, and clinical suspicion of bronchiectasis;
- With poor compliance and expected difficulty in completing the study;
- Other conditions considered inappropriate by the researcher.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
high-dose group
standard dose group
Arm Description
patients take dry suspension of amoxicillin clavulanate potassium 45 mg/kg/ time (amoxicillin) orally twice a day, total daily dose not exceeding 2 g, and the course of treatment is two weeks.
patients take dry suspension of amoxicillin clavulanate potassium 30 mg/kg/ time (amoxicillin) orally twice a day, total daily dose not exceeding 2 g, and the course of treatment is two weeks.
Outcomes
Primary Outcome Measures
cough remission rate
defined as a more than 75% reduction in VCD cough score at the end of the study compared to the baseline score at enrollment, or cough cessation for more than 3 days during the study period.
Secondary Outcome Measures
the absolute change in VCD score
The basic score refers to the average VCD of the first two days (-1 and -2 days). The score at the end of the study was the mean score for the first two days (15,16 days) after the 14-day study period.
the incidence of adverse events
the incidence of any adverse event and severe adverse event
Full Information
NCT ID
NCT04378231
First Posted
April 23, 2020
Last Updated
May 5, 2020
Sponsor
Second Affiliated Hospital of Wenzhou Medical University
1. Study Identification
Unique Protocol Identification Number
NCT04378231
Brief Title
Higher Versus Standard Dose of Amoxicillin-clavulanate in Pediatric PBB
Official Title
Higher Versus Standard Dose of Amoxicillin-clavulanate in Pediatric Protracted Bacterial Bronchitis: a Randomized Controlled Study.
Study Type
Interventional
2. Study Status
Record Verification Date
May 2020
Overall Recruitment Status
Unknown status
Study Start Date
May 2020 (Anticipated)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
July 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital of Wenzhou Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Chronic wet cough is one of the most common symptoms of respiratory diseases in children. Protracted bacterial bronchitis (protracted bacterial bronchitis, PBB) is the most common cause of chronic wet cough in children. Potassium amoxicillin clavulanate is the recommended drug for the treatment of PBB, but there is not enough evidence to date on the dose and course of treatment. investigate the efficacy of different doses of amoxicillin clavulanate sodium in the treatment of chronic bacterial bronchitis in children. The methods of this study are summarized as following:
Screening cases of chronic wet cough in children aged 2 to 6 years old who came to our hospital for treatment. Those diagnosed as PBB were included in this study, after obtaining the written informed consent from their parents or guardians.
The enrolled patients were randomly divided into high-dose (90mg/kg/d) and standard dose (60mg/kg/d) amoxicillin clavulanate potassium treatment group.
Medical history data of enrolled patients and daily cough score data were collected.
Assess the cough remission rate within two weeks and recurrence rate within 6 months in both groups.
Detailed Description
Chronic cough is one of the common reasons for children seeking medical treatment. In children, chronic cough is associated with impaired quality of life, multiple doctor visits, and adverse effects from inappropriate use of medications. Protracted bacterial bronchitis (PBB) is the most common cause of chronic wet cough in children. Most PBB has a good prognosis, but the persistence of PBB can lead to chronic suppurative lung disease, bronchiectasis and chronic obstructive pneumonia. Therefore, PBB must be timely diagnosed, standardized treatment and strict monitoring to avoid the progression of bronchiectasis and chronic obstructive pulmonary disease.
As in children with chronic wet cough, H. influenzae was the most common pathogen cultured from children with PBB. The other commonly detected bacteria are Strep. pneumoniae and M. catarrhalis and while Staphylococcus aureus. Amoxicillin clavulanate is the most commonly recommended drug for the treatment of PBB, but there is no sufficient evidence for the dose and course of treatment. Therefore, the purpose of this study was to elucidate the optimal dose of amoxicillin clavulanate potassium in the treatment of PBB. It is expected that 100 cases will be included and divided into high-dose group and routine dose group. After grouping, the corresponding dose of amoxicillin clavulanate potassium dry suspension will be prescribed according to the grouping conditions. Patients in high-dose group will receive 90mg/kg/d and the regular dose was 60mg/kg/d, which were taken orally twice a day. Medical history data and daily cough score data of enrolled patients were collected to assess the cough remission rate and recurrence rate within 6 months in both groups.
The research content:
Screening cases of chronic wet cough in children aged 2 to 6 years old who came to our hospital for treatment. Those diagnosed with PBB were included in this study after obtaining the written informed consent of their parents or guardians.
The enrolled patients were randomly divided into high-dose (90mg/kg/d) and routine dose (60mg/kg/d) amoxicillin clavulanate potassium treatment group.
Medical history data of enrolled patients and daily cough score data were collected.
Assess the cough remission rate and recurrence rate within 6 months in both groups.
Study design A randomized controlled study for children with protracted bacterial bronchitis
Therapeutic regimens
In high-dose group, patients take dry suspension of amoxicillin clavulanate potassium 45 mg/kg/ time (amoxicillin) orally twice a day, total daily dose not exceeding 2 g, and the course of treatment is two weeks.
In standard dose group, patients take dry suspension of amoxicillin clavulanate potassium 30 mg/kg/ time (amoxicillin) orally twice a day, total daily dose not exceeding 2 g, and the course of treatment is two weeks.
Effect evaluation
Major outcome measure: "cough remission" rate, defined as a more than 75% reduction in verbal category descriptive (VCD) cough score at the end of the study compared to the baseline score at enrollment, or cough cessation for more than 3 days during the study period. The basic score refers to the average VCD of the first two days (-1 and -2 days). The score at the end of the study was the mean score for the first two days (15,16 days) after the 14-day study period.
Secondary outcome measures: the absolute change in VCD score and the incidence of adverse events during the study period.
Safety assessment Safety issues will be evaluated before the enrollment and during the follow-up. it mainly included the analysis of meaningful clinical symptoms and adverse events, and the comparison of laboratory tests before and after the treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Protracted Bacterial Bronchitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
high-dose group
Arm Type
Experimental
Arm Description
patients take dry suspension of amoxicillin clavulanate potassium 45 mg/kg/ time (amoxicillin) orally twice a day, total daily dose not exceeding 2 g, and the course of treatment is two weeks.
Arm Title
standard dose group
Arm Type
Experimental
Arm Description
patients take dry suspension of amoxicillin clavulanate potassium 30 mg/kg/ time (amoxicillin) orally twice a day, total daily dose not exceeding 2 g, and the course of treatment is two weeks.
Intervention Type
Drug
Intervention Name(s)
Amoxicillin-Clavulanate 200 Mg-28.5 Mg Oral dry suspension
Other Intervention Name(s)
Amoxicillin and Clavulanate Potassium for Suspension
Intervention Description
dry suspension of amoxicillin clavulanate potassium
Primary Outcome Measure Information:
Title
cough remission rate
Description
defined as a more than 75% reduction in VCD cough score at the end of the study compared to the baseline score at enrollment, or cough cessation for more than 3 days during the study period.
Time Frame
within two weeks of inclusion
Secondary Outcome Measure Information:
Title
the absolute change in VCD score
Description
The basic score refers to the average VCD of the first two days (-1 and -2 days). The score at the end of the study was the mean score for the first two days (15,16 days) after the 14-day study period.
Time Frame
within two weeks of inclusion
Title
the incidence of adverse events
Description
the incidence of any adverse event and severe adverse event
Time Frame
through their followup completion, an average of half year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Children diagnosed with first-onset PBB
Subjects and their guardians agree to participate in the study and sign an informed consent
Exclusion Criteria:
Seriously delayed development of the nervous system;
With severe underlying diseases: such as severe neuromuscular diseases, immunodeficiency, malnutrition, heart diseases, congenital respiratory system malformation, and other diseases of the heart, brain, liver, kidney and blood system;
Other diseases that can cause chronic wet cough, including chronic rhinitis, sinusitis, interstitial lung disease, and clinical suspicion of bronchiectasis;
With poor compliance and expected difficulty in completing the study;
Other conditions considered inappropriate by the researcher.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiao-guang Hu, MD., PhD.
Phone
08613968893780
Email
topanthu@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Hai-lin Zhang, MD., PhD.
Phone
08613587661971
Email
zhlwz97@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hai-lin Zhang, MD
Organizational Affiliation
Second Affiliated Hospital of Wenzhou Medical Universitiy
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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Higher Versus Standard Dose of Amoxicillin-clavulanate in Pediatric PBB
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