PneumoniaEarly Phase 1PRAPPNCT04963764
Procalcitonin to Reduce Antibiotic Use in Pediatric Pneumonia
A Early Phase 1 study testing Amoxicillin in people with Pneumonia and Pediatric Respiratory Diseases, run by Ann & Robert H Lurie Children's Hospital of Chicago at 3 sites in United States.
Trial summary
This pilot study will evaluate study processes and feasibility of a future large-scale clinical trial that proposes to test whether low-risk children managed as outpatients with community-acquired pneumonia (CAP) and procalcitonin (PCT) levels <0.25 ng/mL treated with placebo have a similar clinical response to those… Read more about this study
- Who is it for?
- Ages 12 to 71 months
- Conditions the study is for
- Pneumonia, Pediatric Respiratory Diseases, Antibiotic Use
- 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
- 5 participants
- Where
- 3 sitesUnited States
- Study dates
- 18 Oct 2021to 27 May 2022
- Phase
- Early Phase 1
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
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 12 to 71 months
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Age 12-71 months; and
- Diagnosis of CAP, defined using established criteria:
- Signs and symptoms of lower respiratory tract infection (LRTI), defined as one or more of the following:
- new or different cough; or
- new or different sputum production; or
- chest pain; or
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- dyspnea/shortness of breath; or
- documented tachypnea; or
- abnormal findings consistent with LRTI on physical examination (e.g., crackles/rales, rhonchi, wheezing) and
- Fever, defined as temperature greater than or equal to 38 degrees C, and
- ED clinician diagnosis of CAP, including intention to treat with antibiotics, and
- Chest radiography suspicious for CAP
- Treatment as an outpatient after ED visit.
- Procalcitonin < 0.25 ng/mL
Who cannot join
- Hospitalization within 7 days preceding study visit; or
- Sustained oxygen saturations <90% with appropriate waveform on oximeter; or
- Incomplete immunization status (<3 doses of Hib and pneumococcal vaccines; or
- Chronic complex medical conditions (chronic heart disease, chronic lung disease (not including asthma), congenital airway or lung malformations, cystic fibrosis, chronic renal disease, protein-losing enteropathy, genetic syndromes, neurocognitive deficits, or metabolic disorders); or
- Conditions that compromise the immune system (HIV, primary immunodeciency, asplenia, sickle cell disease, receipt of hematopoietic stem cell or solid organ trans- plant, immunosuppressive agents, daily corticosteroids for more than 7 consecutive days in past 14 days) ; or
- Systemic antibiotic receipt within the previous 7 days of CAP diagnosis; or
Show all 17Show fewer
- Radiographic findings of complicated pneumonia (moderate-to-large pleural effusion, empyema, abscess, necrotic lung disease) ; or
- Pneumonia known to be due to bacterial source at the time of enrollment, as documented by blood culture or PCR if available, or another clear source of bacterial infection requiring immediate antibiotics; or
- Toxic clinical appearance, sepsis, or critical illness as determined by clinical team at ED presentation; or
- Diagnosed with pneumonia in previous 6 months; or
- Provider diagnosis of bronchiolitis, bronchitis, or aspiration pneumonia; or
- Concomitant asthma exacerbation requiring systemic corticosteroids; or
- Severe drug allergy to amoxicillin; or
- Any other condition that in the judgement of investigators or the clinical team could affect safety of the subject; or
- No access to a telephone or video technology for follow-up; or
- Current enrollment in another clinical trial of an investigational agent; or
- Previous enrollment in this trial.
Trial locations and contacts
3 sites in 1 country.
United States3 sites
Ann & Robert H Lurie Children's Hospital of Chicago
Chicago, Illinois, 60610
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229
The Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, 19104
About this study
This pilot study will evaluate study processes and feasibility of a future large-scale clinical trial that proposes to test whether low-risk children managed as outpatients with community-acquired pneumonia (CAP) and procalcitonin (PCT) levels <0.25 ng/mL treated with placebo have a similar clinical response to those treated with antibiotics and fewer adverse effects.
Read the detailed description
This pilot clinical trial is a 3-site, randomized, placebo-controlled, double-blinded trial assessing the feasibility of comparing amoxicillin to placebo in children 12 months to <6 years of age who present to the ED with Community Acquired Pneumonia (CAP), a procalcitonin (PCT) concentration of <0.25 ng/mL, and who will be treated as outpatients.
Screening and Enrollment This pilot feasibility trial will enroll over a 6-month period and take place at three sites (Ann and Robert H. Lurie Children's Hospital of Chicago, Cincinnati Children's Hospital Medical Center and The Children's Hospital of Philadelphia) that are or were members of the Pediatric Emergency Care Applied Research Network (PECARN). This study aims to enroll 36 patients in total (2 patients per month, per site). Clinical research coordinators (CRCs) at participating EDs will screen potentially eligible patients with respiratory tract symptoms and discuss eligibility with the treating attending physician. If thought to be eligible and a diagnosis of CAP is presumed by the treating physician, the CRC will approach the patient to complete screening procedures. The study will proceed in 2 stages, each with its own informed consent process. During Stage 1, baseline characteristics and serum PCT levels will be ascertained. Stage 2 will consist of a randomized trial of amoxicillin vs. placebo in the subset of patients from Stage 1 that have PCT <0.25 ng/mL.
Randomization After enrollment and confirmation of a PCT <0.25 ng/mL, patients will be randomized to a 10-day course of either amoxicillin (80-100 mg/kg divided BID up to 4,000 mg/day) or placebo. Randomization to amoxicillin or placebo will be at a 1:1 ratio with block sizes of 2 and 4. Patients will be stratified by the clinical site and randomization will be performed through an online system. As a double-blind clinical trial, the study patients and their parents/guardians, investigators and study staff will be blinded to study treatment assignment for the duration of the study.
Study Drug Administration Local investigational drug pharmacies will be provided with active study medication (i.e., amoxicillin) and matching placebo. Site pharmacies at each institution will store study drug and dispense as needed. Study medications will both be liquid reconstituted from powder, and will resemble each other with regards to appearance, favor, consistency and packaging. Study products will be labeled with numerical codes that will maintain allocation concealment. Site investigational pharmacies will be provided with amoxicillin and placebo, in addition to the randomization scheme. The pharmacy will aliquot amoxicillin and placebo into blinded bottles based on randomization scheme.
Follow-up The guardians of participants will be asked to complete a daily symptom diary, using an online data collection form in REDCap, during the first 7 days after the initial Emergency Department study visit. The follow-up will assess patient condition, clinical response, signs or symptoms of clinical deterioration and other adverse effects. The primary outcome will be assessed at day 7 (+/- 2 days), using video chat technology that is standard on most smart phones, tablets, and computers. Video follow-up will be performed by site clinician investigators. In the rare case that a mobile device or computer with video chat technology is not available to the family, the day 7 follow-up will occur by telephone or text through an online system. A final follow-up, performed by site research staff, by telephone call, will occur at Day 21 (+/- 2 days) to assess overall disease course and secondary outcomes.
Data Collection At baseline, demographics, medical history, and history of current illness will be obtained from all participants during stage 1 (pre-randomization). Vital signs will be obtained and a brief physical examination will be performed. After the initial ED visit, patients will record symptoms on daily basis for 6 days via an online data collection form. Follow-up assessments will be completed via telehealth visit or telephone for days 7 and 21. Follow-up visits will collect data regarding symptoms, adverse events and return to medical care, in addition to assessing adherence to study procedures (i.e., medication adherence and daily symptom diary completion). If there is concern for adverse events or deterioration that may warrant medical care, the participant's caregiver will be instructed to contact their primary care physician, emergency department, or call 911, as indicated.
- Being tested
- Amoxicillin, Placebo
- Keywords
- Pediatrics, Pediatric CAP, Pediatric Pneumonia, Antibiotic Use
- Medical subject headings
- Pneumonia, Community-Acquired Pneumonia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
AmoxicillinDrug
Participants will be randomized to receive oral amoxicillin for a standard course (10 days)
PlaceboDrug
Participants will be randomized to receive oral placebo for a standard course (10 days)
| Study group | Role | What they receive |
|---|---|---|
| Placebo | Placebo comparator | Randomization to receive either oral placebo or amoxicillin for a standard course (10 days) Receives: Drug: Placebo |
| Amoxicillin | Active comparator | Randomization to receive either oral amoxicillin or placebo for a standard course (10 days) Receives: Drug: Amoxicillin |
What is being measured
The primary outcome is the main question the study is designed to answer.
Total Pilot Trial Enrollment
Number of patients enrolled in Stage 2 (Randomized Pilot Trial) per site
Measured: Day 7
Secondary outcomes (4)
Consent Rate for Stage 1 (Procalcitonin Ascertainment)
Number of eligible participants approached regarding trial participation who provided informed consent to participate in Stage 1 of the trial compared with number of participants approached for participation
Measured: Measured at completion of pilot trial (6 months)
Rate of Eligible Participants for Stage 2 (Randomized Pilot Trial)
Proportion of participants who received procalcitonin in Stage 1 who had an eligible procalcitonin for Stage 2 (PCT <0.25)
Measured: Measured at completion of pilot trial (6 months)
Consent Rate for Stage 2 (Randomized Pilot Trial)
Number of eligible participants for Stage 2 (PCT <0.25) who provided informed consent to participate in Stage 2 of the trial compared with number of eligible participants approached for participation
Measured: Measured at completion of pilot trial (6 months)
Lost to Follow-Up at Day 7
Number of enrolled participants who did not complete the Day 7 follow-up visit
Measured: Day 7
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Jul 2021
- Study start18 Oct 2021
- Primary completion27 May 2022
- Study completion27 May 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for PneumoniaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Early Phase 1
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Pilot Feasibility Study
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 5 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ann & Robert H Lurie Children's Hospital of Chicago
- Sponsor type
- University, hospital or other
- Collaborators
- Children's Hospital of Philadelphia, Children's Hospital Medical Center, Cincinnati, University of Utah
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04963764
- Sponsor's protocol ID
- 1R34HL153474-01
- Acronym
- PRAPP
- Status last verified
- Oct 2022
- First submitted
- 16 Jun 2021
- Last updated
- 15 Feb 2024
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No: The P-RAPP research team and the PECARN Data Coordinating Center (DCC) at the University of Utah is committed to publicly sharing data for each trial in which we participate in compliance with the NIH's data-sharing policy. As this is a pilot study, a public use dataset will not be developed.
Study at a glance
From the registry record, last updated by the sponsor on 15 Feb 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Procalcitonin to Reduce Antibiotic Use in Pediatric Pneumonia
- ClinicalTrials.gov ID
- NCT04963764
- Acronym / sponsor ID
- PRAPP / 1R34HL153474-01
- Keywords
- Pediatrics, Pediatric CAP, Pediatric Pneumonia, Antibiotic Use
- Phase
- Early Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 5 participants (actual)
- Lead sponsor
- Ann & Robert H Lurie Children's Hospital of ChicagoUniversity, hospital or other
- Collaborators
- Children's Hospital of Philadelphia, Children's Hospital Medical Center, Cincinnati, University of Utah
- Study start
- 18 Oct 2021 (actual)
- Primary completion
- 27 May 2022 (actual)
- Study completion
- 27 May 2022 (actual)
- First posted
- 15 Jul 2021 (actual)
- Results
- Posted 15 Feb 2024
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This pilot study will evaluate study processes and feasibility of a future large-scale clinical trial that proposes to test whether low-risk children managed as outpatients with community-acquired pneumonia (CAP) and procalcitonin (PCT) levels <0.25 ng/mL treated with placebo have a similar clinical response to those treated with antibiotics and fewer adverse effects.
Detailed description
This pilot clinical trial is a 3-site, randomized, placebo-controlled, double-blinded trial assessing the feasibility of comparing amoxicillin to placebo in children 12 months to <6 years of age who present to the ED with Community Acquired Pneumonia (CAP), a procalcitonin (PCT) concentration of <0.25 ng/mL, and who will be treated as outpatients.
Screening and Enrollment This pilot feasibility trial will enroll over a 6-month period and take place at three sites (Ann and Robert H. Lurie Children's Hospital of Chicago, Cincinnati Children's Hospital Medical Center and The Children's Hospital of Philadelphia) that are or were members of the Pediatric Emergency Care Applied Research Network (PECARN). This study aims to enroll 36 patients in total (2 patients per month, per site). Clinical research coordinators (CRCs) at participating EDs will screen potentially eligible patients with respiratory tract symptoms and discuss eligibility with the treating attending physician. If thought to be eligible and a diagnosis of CAP is presumed by the treating physician, the CRC will approach the patient to complete screening procedures. The study will proceed in 2 stages, each with its own informed consent process. During Stage 1, baseline characteristics and serum PCT levels will be ascertained. Stage 2 will consist of a randomized trial of amoxicillin vs. placebo in the subset of patients from Stage 1 that have PCT <0.25 ng/mL.
Randomization After enrollment and confirmation of a PCT <0.25 ng/mL, patients will be randomized to a 10-day course of either amoxicillin (80-100 mg/kg divided BID up to 4,000 mg/day) or placebo. Randomization to amoxicillin or placebo will be at a 1:1 ratio with block sizes of 2 and 4. Patients will be stratified by the clinical site and randomization will be performed through an online system. As a double-blind clinical trial, the study patients and their parents/guardians, investigators and study staff will be blinded to study treatment assignment for the duration of the study.
Study Drug Administration Local investigational drug pharmacies will be provided with active study medication (i.e., amoxicillin) and matching placebo. Site pharmacies at each institution will store study drug and dispense as needed. Study medications will both be liquid reconstituted from powder, and will resemble each other with regards to appearance, favor, consistency and packaging. Study products will be labeled with numerical codes that will maintain allocation concealment. Site investigational pharmacies will be provided with amoxicillin and placebo, in addition to the randomization scheme. The pharmacy will aliquot amoxicillin and placebo into blinded bottles based on randomization scheme.
Follow-up The guardians of participants will be asked to complete a daily symptom diary, using an online data collection form in REDCap, during the first 7 days after the initial Emergency Department study visit. The follow-up will assess patient condition, clinical response, signs or symptoms of clinical deterioration and other adverse effects. The primary outcome will be assessed at day 7 (+/- 2 days), using video chat technology that is standard on most smart phones, tablets, and computers. Video follow-up will be performed by site clinician investigators. In the rare case that a mobile device or computer with video chat technology is not available to the family, the day 7 follow-up will occur by telephone or text through an online system. A final follow-up, performed by site research staff, by telephone call, will occur at Day 21 (+/- 2 days) to assess overall disease course and secondary outcomes.
Data Collection At baseline, demographics, medical history, and history of current illness will be obtained from all participants during stage 1 (pre-randomization). Vital signs will be obtained and a brief physical examination will be performed. After the initial ED visit, patients will record symptoms on daily basis for 6 days via an online data collection form. Follow-up assessments will be completed via telehealth visit or telephone for days 7 and 21. Follow-up visits will collect data regarding symptoms, adverse events and return to medical care, in addition to assessing adherence to study procedures (i.e., medication adherence and daily symptom diary completion). If there is concern for adverse events or deterioration that may warrant medical care, the participant's caregiver will be instructed to contact their primary care physician, emergency department, or call 911, as indicated.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- Pilot Feasibility Study
| Arm | Type | Receives |
|---|---|---|
| Placebo | Placebo comparator | Drug: PlaceboRandomization to receive either oral placebo or amoxicillin for a standard course (10 days) |
| Amoxicillin | Active comparator | Drug: AmoxicillinRandomization to receive either oral amoxicillin or placebo for a standard course (10 days) |
Who may qualify
- Ages
- 12 to 71 months
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (14 listed)
- Age 12-71 months; and
- Diagnosis of CAP, defined using established criteria:
- Treatment as an outpatient after ED visit.
- Procalcitonin < 0.25 ng/mL
Key exclusion criteria (17 listed)
- Hospitalization within 7 days preceding study visit; or
- Sustained oxygen saturations <90% with appropriate waveform on oximeter; or
- Incomplete immunization status (<3 doses of Hib and pneumococcal vaccines; or
- Chronic complex medical conditions (chronic heart disease, chronic lung disease (not including asthma), congenital airway or lung malformations, cystic fibrosis, chronic renal disease, protein-losing enteropathy, genetic syndromes, neurocognitive deficits, or metabolic disorders); or
- Conditions that compromise the immune system (HIV, primary immunodeciency, asplenia, sickle cell disease, receipt of hematopoietic stem cell or solid organ trans- plant, immunosuppressive agents, daily corticosteroids for more than 7 consecutive days in past 14 days) ; or
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| AmoxicillinParticipants will be randomized to receive oral amoxicillin for a standard course (10 days) | Drug | Amoxicillin |
| PlaceboParticipants will be randomized to receive oral placebo for a standard course (10 days) | Drug | Placebo |
Primary outcome
Total Pilot Trial Enrollment
Time frame: Day 7
Number of patients enrolled in Stage 2 (Randomized Pilot Trial) per site
4 secondary outcomes
Consent Rate for Stage 1 (Procalcitonin Ascertainment)
Time frame: Measured at completion of pilot trial (6 months)
Rate of Eligible Participants for Stage 2 (Randomized Pilot Trial)
Time frame: Measured at completion of pilot trial (6 months)
Consent Rate for Stage 2 (Randomized Pilot Trial)
Time frame: Measured at completion of pilot trial (6 months)
Lost to Follow-Up at Day 7
Time frame: Day 7
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Feb 2024.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Individual participant dataSharing planned: No. The P-RAPP research team and the PECARN Data Coordinating Center (DCC) at the University of Utah is committed to publicly sharing data for each trial in which we participate in compliance with the NIH's data-sharing policy. As this is a pilot study, a public use dataset will not be developed.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Early Phase 1 study testing Amoxicillin in people with Pneumonia and Pediatric Respiratory Diseases, run by Ann & Robert H Lurie Children's Hospital of Chicago at 3 sites in United States.
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 14 inclusion and 17 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 15 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in United States. 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.
What does this phase mean?
Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 15 Feb 2024). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
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?
Total Pilot Trial Enrollment (time frame: Day 7). 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 15 Feb 2024.