search
Back to results

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
Second Affiliated Hospital of Wenzhou Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Protracted Bacterial Bronchitis

Eligibility Criteria

2 Years - 6 Years (Child)All SexesDoes not accept healthy volunteers

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

    First Posted
    April 23, 2020
    Last Updated
    May 5, 2020
    Sponsor
    Second Affiliated Hospital of Wenzhou Medical University
    search

    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

    Learn more about this trial

    Higher Versus Standard Dose of Amoxicillin-clavulanate in Pediatric PBB

    We'll reach out to this number within 24 hrs