3 Days Versus 5 Days Amoxicillin for Chest-indrawing Childhood Pneumonia in Malawi

Pneumonia Clinical Trial

Official title:

Double-blind Randomized Controlled Clinical Trial of 3 Days Versus 5 Days Amoxicillin Dispersible Tablets for Chest-indrawing Childhood Pneumonia Among Children 2-59 Months of Age Presenting to Kamuzu Central Hospital in Lilongwe, Malawi

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02678195
• Other study ID #: ITIP2
• Status: Completed
• Phase: Phase 4
• Start date: March 2016
• Est. completion date: December 2019

Study information

• Verified date: February 2021
• Source: Save the Children
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This clinical trial evaluates the duration of treatment of chest-indrawing pneumonia in children. Half the children will receive 3 days of amoxicillin dispersible tablets (DT) and then 2 days of placebo, while the other half will receive 5 days of amoxicillin DT.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 3000
• Est. completion date: December 2019
• Est. primary completion date: April 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Months to 59 Months

Eligibility

Inclusion Criteria:

• Male or female, 2 to 59 months of age.

• History of cough <14 days or difficult breathing with chest-indrawing.

• Ability and willingness of child's caregiver to provide informed consent and to be available for follow-up for the planned duration of the study, including accepting a home visit if he/she fails to return to Kamuzu Central Hospital (KCH) for a scheduled study follow-up visit.

Exclusion Criteria:

• If chest-indrawing observed at screening resolves after bronchodilator challenge, among those with wheeze at screening.

• Severe respiratory distress (e.g., grunting, nasal flaring, head nodding, or severe chest-indrawing).

• Presence of World Health Organization (WHO) Integrated Management of Childhood Illness (IMCI) danger signs including: lethargy or unconsciousness, convulsions, vomiting everything, or inability to drink or breastfeed.

• Hypoxia (SaO2 < 90% on room air, as assessed by a Lifebox pulse oximeter).

• Stridor when calm.

• HIV-1 seropositivity or HIV-1 exposure, assessed as follows:

• An HIV-positive result upon rapid antibody test will exclude any child from this study.

• If a child is less than 12 months or age with a positive rapid test result, the child will be referred to receive additional confirmatory HIV testing (e.g., dried blood spot filter paper test) and follow-up from KCH staff, as per standard of care. Even if the confirmatory HIV testing subsequently shows that child is HIV-negative, he or she will remain excluded from the study.

• If a child is less than 24 months of age and has an HIV-negative result upon rapid antibody test, the child's biological mother's HIV status will need to be assessed. If the mother is HIV-positive, the child will be excluded. If the mother has a documented HIV-negative test result from within the past 6 weeks, the child will be included. If the mother does not have documentation of an HIV-negative test result, she will be tested via rapid antibody testing to determine the child's eligibility for this study.

• If a child is over 24 months of age, an HIV-negative rapid antibody test is required for inclusion in the study.

• Note: If a child has documentation of an HIV-negative test result from within the past 6 weeks, that test result will be used for the child's eligibility assessment according to the algorithm described above.

• Severe acute malnutrition (i.e., weight for height/length < -3 SD, mid-upper arm circumference <115 mm, or edema).

• Possible tuberculosis (coughing for more than 14 days).

• Severe anemia, classified by WHO pocketbook guidelines (i.e., severe palmar pallor or hemoglobin <8.0 g/dL)

• Severe malaria, classified by WHO pocketbook guidelines (e.g., positive malaria rapid diagnostic test (mRDT) with any danger sign, stiff neck, abnormal bleeding, clinical jaundice, or hemoglobinuria)

• Known allergy to penicillin or amoxicillin.

• Receipt of an antibiotic treatment in the 48 hours prior to the study based on caregiver's self-report and/or documentation in child's medical record.

• Hospitalized within 14 days prior to the study.

• Living outside Lilongwe urban area, the study catchment area.

• Any medical or psychosocial condition or circumstance that, in the opinion of the investigators, would interfere with the conduct of the study or for which study participation might jeopardize the child's health.

• Any non-pneumonia acute medical illness which requires antibiotic treatment per local standard of care.

• Participation in a clinical study of another investigational product within 12 weeks prior to randomization or planning to begin participation during this study.

• Prior participation in an Innovative Treatments in Pneumonia (ITIP) study during a previous pneumonia diagnosis.

Related Conditions & MeSH terms

• Pneumonia

Intervention

Drug:
• Amoxicillin
Oral amoxicillin dispersible tablets (DT), 250 mg tablets, given according to age band, two times daily
• Placebo
Placebo dispersible tablets (DT), 250 mg tablets, given according to age band, two times daily

Locations

Country	Name	City	State
Malawi	Bwaila District Hospital	Lilongwe
Malawi	Kamuzu Central Hospital	Lilongwe

Sponsors (3)

Lead Sponsor	Collaborator
Save the Children	University of North Carolina, University of Washington

Country where clinical trial is conducted

Malawi, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of children failing treatment		6 days