Ignite Creation Date:
2025-12-24 @ 1:19 PM
Ignite Modification Date:
2025-12-29 @ 12:40 PM
Study NCT ID:
NCT03416595
Status:
UNKNOWN
Last Update Posted:
2018-07-24
First Post:
2018-01-11
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
A Study on Efficacy of Feeding N1115 Probiotic Supplement to Young Children
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24', 'submissionTracking': {'submissionInfos': [{'releaseDate': '2018-11-26', 'unreleaseDate': '2019-01-10'}, {'resetDate': '2019-04-05', 'releaseDate': '2019-01-10'}], 'estimatedResultsFirstSubmitDate': '2018-11-26'}}}, 'documentSection': {'largeDocumentModule': {'largeDocs': [{'date': '2018-01-11', 'size': 423748, 'label': 'Study Protocol', 'hasIcf': False, 'hasSap': False, 'filename': 'Prot_000.pdf', 'typeAbbrev': 'Prot', 'uploadDate': '2018-01-18T22:17', 'hasProtocol': True}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}, 'primaryPurpose': 'PREVENTION', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'The model is a randomized, double-blinded, parallel, placebo-controlled intervention study to assess effect of N1115 Probiotic Supplement (containing Junlebao Lp. N1115) on gut development in young children. Up to 60 healthy children, between the ages of 6 months and 3 years who were born by caesarean section will be recruited into this study. Participants will be randomly assigned to one of two treatment groups, one group is N1115 Probiotic Supplement intervention which contains Lp. N1115 and maltodextrin, the other group is placebo intervention which contains maltodextrin only.'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 60}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2017-09-18', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2018-01', 'completionDateStruct': {'date': '2018-09-30', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2018-07-22', 'studyFirstSubmitDate': '2018-01-11', 'studyFirstSubmitQcDate': '2018-01-29', 'lastUpdatePostDateStruct': {'date': '2018-07-24', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2018-01-31', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2018-09-30', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Defecation improvement', 'timeFrame': '8 weeks', 'description': 'Compare the defecation condition of child both in intervention group and placebo group by the way of recording the questionnaire each day.\n\nRecord number of defecation and type of stool based on Bristol Stool Scale.'}, {'measure': 'GI symptoms', 'timeFrame': '8 weeks', 'description': 'Compare the gastrointestinal symptoms of child both in intervention group and placebo group by the way of recording the questionnaire each day.\n\nRecord number of flatulence, bloating, cramps and diarrhea compared between child in intervention group and placebo group.'}], 'secondaryOutcomes': [{'measure': 'Fecal microbiota', 'timeFrame': 'study week 0, 4 and 8', 'description': 'Analysis diversity of fecal microbiota, using 16S rRNA gene sequencing, both in intervention group and placebo group to study their gut microbiota composition'}, {'measure': 'Salivary cortisol', 'timeFrame': 'study week 0, 4 and 8', 'description': 'Analysis changes in salivary cortisol, using chemiluminescence immunoassay detection, both in intervention group and placebo group'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['probiotic', 'Lactobacillus paracasei N1115', 'young children'], 'conditions': ['Intestinal Growth of Young Children']}, 'descriptionModule': {'briefSummary': 'The aim of the study is to examine the intervening effects of N1115 Probiotic Supplement (containing Junlebao Lp. N1115) on gut development in young children at the age of 6 month to 3 years by the way of a randomised, double-blinded, parallel, placebo-controlled clinical trial, and to explore the change of intestinal microbiota composition and healthy condition after intervention.', 'detailedDescription': 'N1115 Probiotic Supplement contains Lactobacillus paracasei N1115 \\[Junlebao Lp. N1115\\], a lactobacillus bacteria strain isolated from traditional homemade yogurt in North China. In recent studys feeding Junlebao Lp. N1115 to C57BL/6 mice, the data suggest that Lp. N1115 enhances intestinal development in neonatal mice, and may confer benefits on the growth at early stage of life.\n\nThis study is to investigate if a N1115 Probiotic Supplement product containing Lp. N1115 will improve intestinal health in young children. This randomised, double-blinded, placebo-controlled trial includes two treatment groups which respectively need to recruit 30 volunteers born by cesarean section and aged from 6 months to 3 years. The study group receives N1115 Probiotic Supplement, while the control group receives placebo. The trial lasts for 8 weeks and include four time points of data collection. The stool consistency of children will be recorded everyday, the saliva and stool samples will be collected and analysed.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD'], 'maximumAge': '3 Years', 'minimumAge': '6 Months', 'healthyVolunteers': True, 'eligibilityCriteria': "Inclusion Criteria:\n\n1. Male or female subjects aged ≥ 6 months and ≤ 3 years,\n2. Child was born by caesarean section,\n3. Parent/Guardian has given written informed consent,\n4. Be in generally good health as determined by the investigator.\n\nExclusion Criteria:\n\n1. Are currently taking probiotics or prebiotics, or have taken them in the past 2 weeks,\n2. Unwilling to avoid probiotics/prebiotics for the duration of the study,\n3. Has any food allergies or an allergy or hypersensitivity to any component of the study products, including, milk proteins allergy or cow's milk allergy,\n4. Have a significant acute or chronic coexisting illness (cardiovascular, gastrointestinal, endocrinological, immunological, metabolic or any condition which contraindicates, in the investigators judgement, entry to the study),\n5. Having a condition or taking a medication that the investigator believes would interfere with the objectives of the study, pose a safety risk or confound the interpretation of the study results,\n6. Subjects have taken antibiotics within the past 3 months (history of antibiotic use in previous 6 months recorded),\n7. Subjects may not be receiving treatment involving experimental drugs,\n8. If the subject has been in a recent experimental trial, these must have been completed not less than 60 days prior to this study.\n9. Subjects may not be receiving treatment involving experimental drugs,\n10. Exposure to any non-registered drug product within 30 days prior to screening visit."}, 'identificationModule': {'nctId': 'NCT03416595', 'acronym': 'N1115Baby', 'briefTitle': 'A Study on Efficacy of Feeding N1115 Probiotic Supplement to Young Children', 'organization': {'class': 'INDUSTRY', 'fullName': 'Junlebao Dairy Group Co., Ltd.'}, 'officialTitle': 'A Randomized, Double-blinded, Parallel, Placebo-controlled Study to Investigate the Efficacy of Lb Paracasei [Junlebao Lp. N1115] as a Probiotic to Enhance Gut Development in Young Children', 'orgStudyIdInfo': {'id': 'Lp. N1115 in Young Children'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'ACTIVE_COMPARATOR', 'label': 'N1115 Probiotic Supplement', 'description': 'A probiotic supplement containing Lactobacillus paracasei N1115 \\[Junlebao Lp. N1115\\] Participators, who met inclusion criteria, will receive following product during 8 weeks: N1115 Probiotic Supplement in the form of powder packaged in sachet (one sachet containing 10\\^9 CFU Lp. N1115).', 'interventionNames': ['Dietary Supplement: N1115 Probiotic Supplement']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Placebo control', 'description': 'Dietary Supplement: Placebo Participators, who met inclusion criteria, will receive an identical N1115 Probiotic Supplement looking and tasting placebo.', 'interventionNames': ['Dietary Supplement: placebo']}], 'interventions': [{'name': 'N1115 Probiotic Supplement', 'type': 'DIETARY_SUPPLEMENT', 'otherNames': ['Junlebao Lp. N1115'], 'description': 'Participators will receive a sachet each day during 8 weeks. The contents of the sachet should be added to warm water or milk, mixed until fully dissolved and served within 15 minutes.', 'armGroupLabels': ['N1115 Probiotic Supplement']}, {'name': 'placebo', 'type': 'DIETARY_SUPPLEMENT', 'description': 'Participators will receive a sachet each day during 8 weeks. The contents of the sachet should be added to warm water or milk, mixed until fully dissolved and served within 15 minutes.', 'armGroupLabels': ['Placebo control']}]}, 'contactsLocationsModule': {'locations': [{'city': 'Cork', 'state': 'Blackrock', 'country': 'Ireland', 'facility': 'Atlantia Clinical Food Trials', 'geoPoint': {'lat': 51.89797, 'lon': -8.47061}}], 'overallOfficials': [{'name': 'Barry Skillington, Postgraduate', 'role': 'STUDY_DIRECTOR', 'affiliation': 'The director of this clinical trial in Ireland'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'UNDECIDED'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Junlebao Dairy Group Co., Ltd.', 'class': 'INDUSTRY'}, 'collaborators': [{'name': 'Atlantia Food Clinical Trials', 'class': 'INDUSTRY'}, {'name': 'Teagasc', 'class': 'INDUSTRY'}], 'responsibleParty': {'type': 'SPONSOR'}}}, 'annotationSection': {'annotationModule': {'unpostedAnnotation': {'unpostedEvents': [{'date': '2018-11-26', 'type': 'RELEASE'}, {'date': '2019-01-10', 'type': 'UNRELEASE'}, {'date': '2019-01-10', 'type': 'RELEASE'}, {'date': '2019-04-05', 'type': 'RESET'}], 'unpostedResponsibleParty': 'Junlebao Dairy Group Co., Ltd.'}}}}