Ignite Creation Date:
2025-12-25 @ 2:22 AM
Ignite Modification Date:
2025-12-26 @ 12:53 AM
Study NCT ID:
NCT03446534
Status:
UNKNOWN
Last Update Posted:
2018-04-11
First Post:
2018-02-17
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
The Norwegian Antibiotics for Pneumonia in Children Study
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D011014', 'term': 'Pneumonia'}], 'ancestors': [{'id': 'D012141', 'term': 'Respiratory Tract Infections'}, {'id': 'D007239', 'term': 'Infections'}, {'id': 'D008171', 'term': 'Lung Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D000658', 'term': 'Amoxicillin'}], 'ancestors': [{'id': 'D000667', 'term': 'Ampicillin'}, {'id': 'D010400', 'term': 'Penicillin G'}, {'id': 'D010406', 'term': 'Penicillins'}, {'id': 'D047090', 'term': 'beta-Lactams'}, {'id': 'D007769', 'term': 'Lactams'}, {'id': 'D000577', 'term': 'Amides'}, {'id': 'D009930', 'term': 'Organic Chemicals'}, {'id': 'D013457', 'term': 'Sulfur Compounds'}, {'id': 'D006574', 'term': 'Heterocyclic Compounds, 2-Ring'}, {'id': 'D000072471', 'term': 'Heterocyclic Compounds, Fused-Ring'}, {'id': 'D006571', 'term': 'Heterocyclic Compounds'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE4'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'The study is a phase IV double-blind, placebo-controlled, multicenter, nationwide, randomized superiority trial of amoxicillin versus placebo in children aged 1-5 years of age with a lower respiratory infection.'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 884}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'RECRUITING', 'startDateStruct': {'date': '2018-03-07', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2018-04', 'completionDateStruct': {'date': '2020-12', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2018-04-10', 'studyFirstSubmitDate': '2018-02-17', 'studyFirstSubmitQcDate': '2018-02-23', 'lastUpdatePostDateStruct': {'date': '2018-04-11', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2018-02-26', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2020-05', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Therapy Failure', 'timeFrame': 'Within 7 days after inclusion', 'description': 'Therapy failure as defined by attending physician, leading to end of intervention and administration of open-label antibiotics'}], 'secondaryOutcomes': [{'measure': 'Thereapy failure leading to intravenous antibiotic therapy', 'timeFrame': 'Within 7 days after inclusion', 'description': 'Therapy failure as defined by attending physician, leading to intravenous antibiotic therapy'}, {'measure': 'Duration of fever', 'timeFrame': 'Up to 21 days after inclusion', 'description': 'Duration of fever'}, {'measure': 'Duration of symptoms of pneumonia', 'timeFrame': 'Up to 21 days after inclusion', 'description': 'Duration of cough or respiratory distress (tachypnoe, retractions, grunting respiration or nasal flaring.'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['pneumonia', 'pre-school children', 'antibiotics', 'amoxicillin'], 'conditions': ['Pneumonia Childhood', 'Lower Respiratory Tract Infection']}, 'descriptionModule': {'briefSummary': 'This study evaluates the effect of amoxicillin in the treatment of lower airway infections in preschool children. Half of the patients will receive amoxicillin, while the other half will receive placebo.', 'detailedDescription': 'The overall objective of the study is to determine if antibiotic therapy is beneficial in children with pneumonia who do not have a highly suspicious bacterial infection, such as in lobar pneumonia.\n\nSecondary objective is to determine whether antibiotic use influence the microbial flora, including antibiotic resistance, in the airways in the short or medium long term.\n\nThe study is a phase IV double-blind, placebo-controlled, multicenter, nationwide, randomized superiority trial of amoxicillin versus placebo in children aged 1-5 years of age with a lower respiratory infection.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD'], 'maximumAge': '59 Months', 'minimumAge': '12 Months', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n1. Age 12-59 months\n2. Fever:\n\n a. Temperature ≥ 38.0 at inclusion or reported within the last 24 hours\n3. Tachypnoe, age specific 12-17mnd ≥ 46 breaths per minute 18-23mnd ≥ 40 breaths per minute 24-35mnd ≥ 34 breaths per minute 36-47mnd ≥ 29 breaths per minute 48-59mnd ≥ 27 breaths per minute\n4. ≥ 1 sign of lower airway inflammation\n\n 1. Cough (at inclusion or reported within the last 6 hours)\n 2. Chest retractions (jugular, intercoastally or subcoastally)\n 3. Grunting respiration\n 4. Nasal flaring\n 5. Crepitations by pulmonary auscultation\n 6. Hypoxia (SpO2 ≤ 90%)\n5. Weight between 6.0 and 28.0 kg. • Signed informed consent and expected cooperation of the patients for the treatment and follow up must be obtained and documented according to ICH GCP, and national/local regulations\n\nExclusion Criteria:\n\n1. Clinical suspicion of bacterial pneumonia based upon a temperature ≥39.0°C and at least one of the following:\n\n 1. Bronchial breathing sounds\n 2. Unilaterally decreased breath sounds or unilateral percussion dullness\n 3. Pulmonary lobar consolidation and/or radiological high suspicion of empyema on chest x-ray if this is obtained prior to inclusion in the trial.\n2. Evidence of any bacterial infection requiring systemic antibiotics, including, but not exclusively:\n\n 1. Clinical septicaemia\n 2. Urinary tract infection\n 3. Meningitis\n3. Systemic antibiotics received within the last 7 days\n4. Pulmonary lobar consolidation and/or radiological high suspicion of empyema on chest x-ray if this is obtained prior to inclusion in the trial.\n5. History of any serious underlying disease that can increase the risk of bacterial pulmonary infections, including but not limited to:\n\n 1. Haematological or oncological\n 2. Immunodeficiency\n 3. Congenital heart disease\n 4. Neuromuscular impairment\n 5. Development disorder, including Downs syndrome\n 6. Bronchopulmonary dysplasia, cystic fibrosis, primary ciliary dyskinesia, poorly controlled asthma or other severe chronic lung diseases\n6. Signs of lower obstructive airways with both of the following present by auscultation:\n\n 1. prolonged expiration and\n 2. generalised expiratory wheeze\n7. Stridor by auscultation.\n8. History of known or suspected adverse reactions to amoxicillin, or any other betalactam\n9. Participating in another trial that might affect the current study\n10. Any reason why, in the opinion of the investigator, the patient should not participate (e.g. not able to comply with study procedures)'}, 'identificationModule': {'nctId': 'NCT03446534', 'acronym': 'NAPiC', 'briefTitle': 'The Norwegian Antibiotics for Pneumonia in Children Study', 'organization': {'class': 'OTHER', 'fullName': 'Oslo University Hospital'}, 'officialTitle': 'The Norwegian Antibiotics for Pneumonia in Children Study', 'orgStudyIdInfo': {'id': '2017/1863'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Amoxicillin', 'description': 'Amoxicillin 100mg/ml mixture (Imacillin), 0.25ml/kg every 8 hours for 7 days.', 'interventionNames': ['Drug: Amoxicillin']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Placebo', 'description': 'Placebo mixture 0.25ml/kg every 8 hours for 7 days', 'interventionNames': ['Drug: Placebos']}], 'interventions': [{'name': 'Amoxicillin', 'type': 'DRUG', 'otherNames': ['Imacillin'], 'description': 'Imacillin mixture', 'armGroupLabels': ['Amoxicillin']}, {'name': 'Placebos', 'type': 'DRUG', 'description': 'Placebo manufactured to mimic amoxicillin mixture (Imacillin)', 'armGroupLabels': ['Placebo']}]}, 'contactsLocationsModule': {'locations': [{'zip': '6017', 'city': 'Ålesund', 'status': 'RECRUITING', 'country': 'Norway', 'contacts': [{'name': 'Torbjørn Nag', 'role': 'CONTACT', 'email': 'torbjorn.nag@helse-mr.no', 'phone': '41638349'}, {'name': 'Torbjørn Nag, MD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Ålesund Hospital Trust', 'geoPoint': {'lat': 62.47225, 'lon': 6.15492}}, {'zip': '5021', 'city': 'Bergen', 'status': 'NOT_YET_RECRUITING', 'country': 'Norway', 'contacts': [{'name': 'Håvard Trønnes, PhD', 'role': 'CONTACT', 'email': 'havard.tronnes@ihelse.net', 'phone': '95777862'}, {'name': 'Håvard Trønnes, PhD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Haukeland University Hospital', 'geoPoint': {'lat': 60.39299, 'lon': 5.32415}}, {'zip': '8005', 'city': 'Bodø', 'status': 'RECRUITING', 'country': 'Norway', 'contacts': [{'name': 'Bjørg Evjenth', 'role': 'CONTACT', 'email': 'bjorg.evjenth@gmail.com', 'phone': '99258992'}, {'name': 'Bjørg Evjenth, PhD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Nordlandssykehuset Bodø', 'geoPoint': {'lat': 67.28267, 'lon': 14.37513}}, {'zip': '1714', 'city': 'Grålum', 'status': 'NOT_YET_RECRUITING', 'country': 'Norway', 'contacts': [{'name': 'Jon Olav Hunderi, MD', 'role': 'CONTACT', 'email': 'jon.olav.gjengsto.hunderi@so-hf.no', 'phone': '91880816'}, {'name': 'Jon Olav Hunderi, M.D.', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Østfold Hospital Trust', 'geoPoint': {'lat': 59.29048, 'lon': 11.06668}}, {'zip': '1478', 'city': 'Lørenskog', 'status': 'NOT_YET_RECRUITING', 'country': 'Norway', 'contacts': [{'name': 'Christopher Inchley', 'role': 'CONTACT', 'email': 'christopher.inchley@medisin.uio.no', 'phone': '90069276'}, {'name': 'Christopher Inchley, PhD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Akershus University Hospital'}, {'zip': '0424', 'city': 'Oslo', 'status': 'RECRUITING', 'country': 'Norway', 'contacts': [{'name': 'Håvard O Skjerven, PhD', 'role': 'CONTACT', 'email': 'h.o.skjerven@medisin.uio.no', 'phone': '41020249'}, {'role': 'CONTACT', 'email': 'h.o.skjerven@medisin.uio.no', 'phoneExt': 'Skjerven'}, {'name': 'Håvard O Skjerven, PhD', 'role': 'SUB_INVESTIGATOR'}, {'name': 'Per Kristian Knudsen, MD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Oslo University of Oslo', 'geoPoint': {'lat': 59.91273, 'lon': 10.74609}}, {'zip': '4011', 'city': 'Stavanger', 'status': 'RECRUITING', 'country': 'Norway', 'contacts': [{'name': 'Knut Øymar, PhD', 'role': 'CONTACT', 'email': 'knut.oymar@sus.no', 'phone': '41633426'}, {'name': 'Knut Øymar, PhD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Stavanger University Hospital', 'geoPoint': {'lat': 58.97005, 'lon': 5.73332}}, {'zip': '9038', 'city': 'Tromsø', 'status': 'NOT_YET_RECRUITING', 'country': 'Norway', 'contacts': [{'name': 'Claus Klingenberg', 'role': 'CONTACT', 'email': 'claus.klingenberg@unn.no', 'phone': '91563167'}, {'name': 'Claus Klingenberg', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'University Hospital of Northern Norway', 'geoPoint': {'lat': 69.6489, 'lon': 18.95508}}, {'zip': '7030', 'city': 'Trondheim', 'status': 'NOT_YET_RECRUITING', 'country': 'Norway', 'contacts': [{'name': 'Henrik Döllner, PhD', 'role': 'CONTACT', 'email': 'henrik.dollner@ntnu.no', 'phone': '47667169'}, {'name': 'Henrik Döllner, PhD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'St. Olav University Hospital', 'geoPoint': {'lat': 63.43049, 'lon': 10.39506}}], 'centralContacts': [{'name': 'Håvard O Skjerven, PhD', 'role': 'CONTACT', 'email': 'h.o.skjerven@medisin.uio.no', 'phone': '+47 41020249'}, {'name': 'Per Kristian Knudsen, MD', 'role': 'CONTACT', 'email': 'perkristiank@gmail.com', 'phone': '+4791631421'}], 'overallOfficials': [{'name': 'Håvard O Skjerven', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Oslo University Hospital'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Oslo University Hospital', 'class': 'OTHER'}, 'collaborators': [{'name': 'Ostfold Hospital Trust', 'class': 'OTHER'}, {'name': 'Helse Stavanger HF', 'class': 'OTHER_GOV'}, {'name': 'Haukeland University Hospital', 'class': 'OTHER'}, {'name': 'Alesund Hospital', 'class': 'OTHER'}, {'name': 'St. Olavs Hospital', 'class': 'OTHER'}, {'name': 'Nordlandssykehuset HF', 'class': 'OTHER'}, {'name': 'University Hospital of North Norway', 'class': 'OTHER'}, {'name': 'University Hospital, Akershus', 'class': 'OTHER'}, {'name': 'Norwegian Institute of Public Health', 'class': 'OTHER_GOV'}, {'name': 'Klinbeforsk', 'class': 'OTHER'}], 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'Consultant', 'investigatorFullName': 'Håvard Ove Skjerven', 'investigatorAffiliation': 'Oslo University Hospital'}}}}