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Acute Respiratory InfectionsNCT00851487

Trial of Amoxicillin Compared With Placebo for Pneumonia in Children Aged 2-59 Months

A study testing Amoxicillin in people with Acute Respiratory Infections and Pneumonia, run by Pakistan Institute of Medical Sciences at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Many children with "non-severe pneumonia" (cough and fast breathing) have neither clinical pneumonia as assessed by physicians nor pneumonia on chest radiographs. Inappropriate use of antibiotics for these cases is leading to resistant strains of bacteria in the community. Read more about this study

Who is it for?
Ages 2 to 59 months
Conditions the study is for
Acute Respiratory Infections, Pneumonia
What is being tested?
Amoxicillin
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
900 participants
Where
1 sitePakistan
Study dates
Jan 2006to Apr 2008
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 2 to 59 months
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Children aged 2 to 59 months attending the outpatient's clinics of participating sites
  • WHO defined non-severe pneumonia
  • Accessibility for follow-up
  • Written informed consent by a parent or legal guardian

Who cannot join

  • WHO signs of severe pneumonia recognised by lower chest wall retraction. Children who present with wheezing will be evaluated for lower chest wall indrawing after treatments with nebulised salbutamol. WHO signs of very severe disease/pneumonia defined as any of the following:
  • Cyanosis
  • Inability to drink
  • Convulsions
  • Abnormally sleepy or difficult to wake
  • Severe malnutrition recognised by weight for age less than third percentile by the NCHS (National Child Health Statistics) growth chart and/or oedema (see chart).
Show all 16Show fewer
  • All patients with a previous history of 3 or more episodes of wheeze or diagnosed to have asthma.
  • Known or clinically recognisable congenital heart disease with cyanosis or, congestive heart failure or cardiomegaly.
  • Known or clinically recognisable acute/chronic organ system disorders including jaundice, nephrotic syndrome, severe anaemia manifested as extreme pallor etc.
  • Other infectious conditions requiring antibiotic therapy at the day of contact including meningitis, tuberculosis, dysentery, osteomyelitis, septic arthritis etc.
  • Children who have taken the appropriate doses of WHO-recommended dose of anti microbial drug for 48 hours prior to presentation.
  • A history of hospitalization in the past 2 weeks
  • Measles or a history of measles within the last month: Measles recognized by presence of fever with rash, and conjunctivitis.
  • Prior enrolment in the current trial.
  • Known penicillin allergy, including a history of rash, urticaria, or anaphylactic symptoms.
  • The children living outside the municipal limits of the city who cannot be followed up.

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • ARI Research Cell, Children Hospital, PIMS

    Islamabad, Federal Capital, 44000

Other trials in Pakistan

About this study

Official title: A Randomized Multicentre Double Blind Trial of Amoxicillin Compared With Placebo for Treatment of WHO Defined Non-Severe Pneumonia in Children Aged 2-59 Months: NARIMA Study Group

Many children with "non-severe pneumonia" (cough and fast breathing) have neither clinical pneumonia as assessed by physicians nor pneumonia on chest radiographs. Inappropriate use of antibiotics for these cases is leading to resistant strains of bacteria in the community. Evidence shows that almost 50% of antibiotic prescription is unnecessary.As over half of antibiotic prescription for ARI are not necessary since most of these infections are viral and do not respond to antibiotic therapy which will be source of resistance in the community.

To address this issue the investigators conducted this randomized, double blind placebo controlled clinical trial of oral Amoxicillin versus placebo in children with non-severe pneumonia taking into account all the necessary safety precautions for their well being.

The study hypothesis was that the clinical outcome of children 2 to 59 months of age with cough and fast breathing (WHO defined non-severe pneumonia) with or without wheezing is equivalent, whether they are treated with amoxicillin or placebo.

Read the detailed description

Pneumonia is one of the major cause of childhood morbidity and mortality in developing countries. Burden of acute respiratory infections (ARI) is high with an estimated 5-7 episodes in under 5 population every year resulting in 2 million deaths. However, most of these are due to severe bacterial pneumonia.

In order to reduce pneumonia related deaths in communities where qualified personnel and diagnostic facilities are often not available WHO developed management guidelines based on simple clinical signs followed by empirical treatment. All children with cough and fast breathing are classified into management categories: Children with fast breathing only are classified as having non-severe pneumonia requiring oral antibiotic at home, children who have lower chest indrawing and /or general danger signs (GDS) are classified as severe pneumonia, and very severe pneumonia respectively. Both these groups require referral to a hospital and injectible antibiotic therapy. These guidelines have shown to effectively reduce ARI related mortality by 34% (?) in communities where they have been successfully implemented.

However, there are certain concerns regarding these guidelines. It is felt that using the sign of fast breathing alone for prescribing antibiotic may not be the most judicious thing from a public health perspective as it may lead to the spread of antibiotic resistance. Fast breathing could be due to many other causes not related to pneumonia.

There are many factors affecting the respiratory rate I children. Children with fever will have elevated respiratory rates in any case. Although WHO guidelines recommend that respiratory rate must be counted when child is afebrile, calm and preferably sleeping. In real life such practice is not always possible.

Another issue is the children with cough and fast breathing who have wheezing. In many developing countries wheeze is commonly associated with fast and difficult breathing. Data from the developed countries shows that wheeze is more common in viral than bacterial infections. Likewise, data from the developing countries has shown that viruses, especially respiratory syncytial virus (RSV), are isolated more frequently than bacteria from children with episodes of acute lower respiratory tract infections. A randomized trial of infants with bronchiolitis and pneumonia found no difference in clinical outcome in children with antibiotics compared with placebo(ref?). Wheeze has long been unaddressed and is one of the major cause for overuse of antibiotics. Evidence shows that three cycles of inhaled bronchodilator was found to be associated with a significant decrease in respiratory rate leading to revised classification of "no pneumonia" in these children. It has convincingly shown that majority of these children continue to do well when sent home without an antibiotic.

Though fast breathing is an important indicator for clinical diagnosis of pneumonia it cannot distinguish viral from bacterial pathogens Controversy still exists concerning the relative importance of viral and bacterial pathogens so a reliable distinction between bacterial and viral infection has yet to be established and this issue has raised a lot of questions for the programme managers, senior researchers and technical experts, which still need to be answered.

Many children with "non-severe pneumonia" (cough and fast breathing) have neither clinical pneumonia as assessed by physicians nor pneumonia on chest radiographs. Inappropriate use of antibiotics for these cases is leading to resistant strains of bacteria in the community. Evidence shows that almost 50% of antibiotic prescription is unnecessary. As over half of antibiotic prescription for ARI are not necessary since most of these infections are viral and do not respond to antibiotic therapy which will be source of resistance in the community. When resistant bacteria become common, we may begin to see treatment failures in the children with severe pneumonia who really require an effective antibiotic. It is imperative to have the knowledge of likely cause and pattern of pneumonia which could be utilized to better understand the model of antibiotic resistance.

For the above stated reasons, there is a need to further elaborate the role of antibiotics in children with cough and fast breathing. To address this issue we conducted this randomized, double blind placebo controlled clinical trial of oral Amoxicillin versus placebo in children with non-severe pneumonia taking into account all the necessary safety precautions for their well being. The primary objective was to determine whether children aged 2 to 59 months with cough and fast breathing, with or without wheezing, but no evidence of WHO defined severe illness, have equivalent clinical failure at 72 hours of therapy when treated with Amoxicillin compared to placebo.

Being tested
Amoxicillin, Placebo
Keywords
ARI, LRTI
Medical subject headings
Pneumonia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AmoxicillinDrug

    Also called Amoxycillin

    Oral Amoxicillin 15 mg/kg/dose 8 hourly

  • PlaceboDrug

    The placebo was similar in colour, consistency and volume as oral amoxicillin

Study groups in NCT00851487
Study groupRoleWhat they receive
AmoxicillinExperimentalOral amoxicillin in the dose of 15 mg/kg/dose 8 hourly was given as an active drug
Receives: Drug: Amoxicillin
PlaceboPlacebo comparatorThe placebo was similar in colour, consistency and volume as oral amoxicillin
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The primary outcome measure was treatment failure within the first 72 hours of therapy

    Measured: 3 days

Secondary outcomes (1)
  1. The secondary outcome measure was treatment failure on the third follow-up (day 5) plus non-improvement

    Measured: 5 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Feb 2009 (estimated)
  2. Study startJan 2006
  3. Primary completionApr 2008
  4. Study completionApr 2008

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
900 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00851487
Sponsor's protocol ID
NARIMA Study Group
Status last verified
Feb 2009
First submitted
25 Feb 2009
Last updated
26 Feb 2009
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A study testing Amoxicillin in people with Acute Respiratory Infections and Pneumonia, run by Pakistan Institute of Medical Sciences at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 16 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Feb 2009. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The primary outcome measure was treatment failure within the first 72 hours of therapy (time frame: 3 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Feb 2009.

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