Twice Daily Treatment With Amoxicillin for Non-severe Community Acquired Pneumonia.

Community-acquired Pneumonia Clinical Trial

Official title:

Treatment of Non-severe Community Acquired Pneumonia With Twice Daily Compared to Thrice Daily Regimen- A Non-inferiority Pragmatic Randomized-controlled Trial.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03031210
• Other study ID #: BID pneumonia
• Status: Recruiting
• Phase: Phase 2/Phase 3
• Start date: June 11, 2017
• Est. completion date: June 1, 2024

Study information

• Verified date: November 2023
• Source: St. Justine's Hospital
• Contact: Jocelyn Gravel, MD
• Phone: 514-345-4931
• Email: graveljocelyn[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this study will be to evaluate whether a twice-daily antibiotic regimen is non-inferior to a thrice-daily regimen for the treatment of non-severe community acquired pneumonia in children presenting at a paediatric Emergency Department (ED).

Description:

A single-center, non-blinded, pragmatic, randomized-controlled, non-inferiority clinical trial will be conducted in an urban, university-affiliated, tertiary care pediatric hospital ED. All patients three months old to 18 years of age who had symptoms and signs suggestive of non-severe community acquired pneumonia based on respiratory complaints and a pulmonary infiltrate identified by trained paediatricians or emergency physicians will be eligible to the present study. Study participants will be randomly allocated to receive either amoxicillin (90mg/kg per day) in twice or thrice daily regimen. Primary outcome will be treatment failure within 10 days of enrolment as defined by hospitalisation, need for a change in antibiotic (persistence of fever at 72 hours, clinical deterioration, comorbid condition or development of serious adverse reactions) and death. ED revisits within 72 hours, second course of antibiotic and clinical recurrence rates will be evaluated in the follow-up assessments as well as percent of adverse events encountered, number of days missed (work, school or daycare), coverage vaccination rate, protocol adherence and patient and parental satisfaction. The primary analysis will use an intention-to-treat approach. Per-protocol analysis will also be carried to compare the failure rate. Accounting to a maximal 10% drop-off rate, a sample size of 685 participants per arm was calculated to have a power of 90% to identify a difference of ≤ 5% with an alpha value of 0.05.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 1370
• Est. completion date: June 1, 2024
• Est. primary completion date: June 1, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 3 Months to 18 Years

Eligibility

Inclusion Criteria:

• All patients 3 months to 18 years of age attending the pediatric ED and diagnosed with a non-severe pneumonia, will be considered for enrolment. More precisely, the following inclusion criteria will be required:

1. Presence of respiratory symptoms (cough and/or dyspnea)

2. Presence of signs of pneumonia (tachypnea, abnormal breath sounds, crackles)

3. Presence of fever

4. Positive chest radiography as interpreted by the treating physician

Exclusion Criteria:

• Any danger signs associated with pneumonia (severe indrawing, shock or severe dehydration, empyema, important pleural effusion, pulmonary abcess or pneumatocoele)

• History of anaphylactic or allergic reaction to penicillin or amoxicillin according to the treating physician.

• History of a serious nonimmunoglobulin E-mediated reactions (eg, Stevens-Johnson syndrome or toxic epidermal necrolysis) attributed to amoxicilin.

• Caregiver unable to provide consent (language barrier or lack of caregiver presence)

• Underlying unstable chronic illness (ie. cystic fibrosis, immune suppression, active tuberculosis, bronchiectasis or active pulmonary malignancies)

• Persistent/chronic pneumonia syndromes (with symptoms for >2 weeks), suspected by the physician to be caused by atypical pathogens, hospital- acquired pneumonia (been hospitalized within 2 weeks prior to enrolment), aspiration pneumonia or recurrent pneumonias.

• Any history of receiving amoxicillin within the past month

• Need hospitalisation for any other reasons (ie. persistent vomiting, severe life-threatening infection such as septicaemia or meningitis requiring intravenous antimicrobial agents)

• Previous participation in study

Related Conditions & MeSH terms

• Community-acquired Pneumonia
• Pneumonia

Intervention

Drug:
• Amoxicillin
(90 mg/kg/day) twice daily

Locations

Country	Name	City	State
Canada	CHU Sainte-Justine	Montreal	Quebec

Sponsors (1)

Lead Sponsor	Collaborator
St. Justine's Hospital

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical failure within 10 days of enrolment	As a primary outcome, clinical failure will be defined by any of the following occurring within 10 days of enrolment: Death or hospitalisation; A need for a change in antibiotic according to the treating physician. In our settings, common reasons to change antibiotic are: Persistence of fever at 72h; Clinical deterioration: • Clinical deterioration will include the development of lower chest-wall indrawing, central cyanosis, stridor while calm, or danger signs as defined by: inability to drink or breastfeed, convulsions, persistent vomiting, lethargy, or unconsciousness at any time during a child's treatment.; Development of a comorbid condition such as a meningitis, bacteriemia, osteomyelitis or septic arthritis; Allergic reaction	Day 10 (after enrolment)
Secondary	Emergency department revisit within 72 hours	Return to the emergency department in the following 72 hours	72 hours
Secondary	Second course of antibiotic	Necessity of second course of antibiotics	1 month
Secondary	Clinical recurrence	Another diagnosis of pneumonia	1 month
Secondary	Adverse events	Any adverse event	10 days
Secondary	Number of working days missed by caregivers or school/daycare days missed by patients	Total number of days missed by caregivers or school/daycare days missed by the parents	1 month
Secondary	Patient's and parents satisfaction with the discharge instructions' provided and the ease of administration	Measured on a likert scale through a telephone survey	10 days