Viewing Study NCT05073393


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Study NCT ID: NCT05073393
Status: COMPLETED
Last Update Posted: 2022-08-23
First Post: 2021-10-08
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Effect of Probiotics on Oral Homeostasis During Sugar Stress
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D003731', 'term': 'Dental Caries'}, {'id': 'D005891', 'term': 'Gingivitis'}], 'ancestors': [{'id': 'D017001', 'term': 'Tooth Demineralization'}, {'id': 'D014076', 'term': 'Tooth Diseases'}, {'id': 'D009057', 'term': 'Stomatognathic Diseases'}, {'id': 'D007239', 'term': 'Infections'}, {'id': 'D005882', 'term': 'Gingival Diseases'}, {'id': 'D010510', 'term': 'Periodontal Diseases'}, {'id': 'D009059', 'term': 'Mouth Diseases'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR'], 'maskingDescription': 'Computerized randomization only known to the principal investigator, who are not directly involved in data collection or data analysis'}, 'primaryPurpose': 'PREVENTION', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'Double blinded randomized clinical trial with a test and placebo group'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 80}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2021-11-03', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2022-08', 'completionDateStruct': {'date': '2022-06-01', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2022-08-22', 'studyFirstSubmitDate': '2021-10-08', 'studyFirstSubmitQcDate': '2021-10-08', 'lastUpdatePostDateStruct': {'date': '2022-08-23', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2021-10-11', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2021-12-17', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Changes in microbial composition in dental plaque', 'timeFrame': 'Baseline vs. Day 14 and Day 28', 'description': 'Changes in alpha and beta diversity of microbial composition'}], 'secondaryOutcomes': [{'measure': 'Changes in clinical parameters', 'timeFrame': 'Baseline vs. Day 14 and Day 28', 'description': 'Changes in levels of dental plaque and gingival inflammation'}, {'measure': 'Changes in salivary levels of inflammatory cytokines', 'timeFrame': 'Baseline vs. Day 14 and Day 28', 'description': 'Changes in mean salivary levels of selected inflammatory cytokines'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Dental Caries', 'Probiotics', 'Gingivitis']}, 'descriptionModule': {'briefSummary': 'The present study is a double-blinded randomized clinical trial with a duration of 28 days.', 'detailedDescription': 'The present study is a double-blinded randomized clinical trial with a duration of 28 days.\n\n80 orally and systemically healthy participant will be allocated in the test (probiotic) and the control (placebo) group at baseline.\n\nThe intervention is sugar stress, which will be applied at baseline and continue through day 14, followed by 14 days without sugar stress.\n\nClinical measurements and sampling will be performed at baseline, day 14 and day 28\n\nPrimary endpoint: Changes in microbial composition.\n\nSecondary endpoints: Changes in clinical and immunological parameters'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT'], 'maximumAge': '30 Years', 'minimumAge': '18 Years', 'healthyVolunteers': True, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* age \\> 18 yrs.\n\nExclusion Criteria:\n\n* Presence of oral diseases i.e. gingivitis, periodontitis and dental caries\n* Current smokers\n* Any systemic diseases and current use of any medication with known effect on oral health\n* Use of systemic antibiotics within the latest three months.\n* Age \\< 18 yrs., and age \\> 30 yrs.'}, 'identificationModule': {'nctId': 'NCT05073393', 'briefTitle': 'Effect of Probiotics on Oral Homeostasis During Sugar Stress', 'organization': {'class': 'OTHER', 'fullName': 'University of Copenhagen'}, 'officialTitle': 'Effect of Probiotics on Oral Homeostasis During Sugar Stress', 'orgStudyIdInfo': {'id': 'UCPH_01_005'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Probiotic', 'description': 'In this group participants will receive probiotic supplements twice a day (morning and evening) for at period of 28 days (14 days with sugar stress followed by 14 days without sugar stress).', 'interventionNames': ['Behavioral: Sugar stress']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Placebo', 'description': 'In this group participants will receive placebo twice a day (morning and evening) for at period of 28 days (14 days with sugar stress followed by 14 days without sugar stress).', 'interventionNames': ['Behavioral: Sugar stress']}], 'interventions': [{'name': 'Sugar stress', 'type': 'BEHAVIORAL', 'description': 'Sucrose rinsing for 14 days (8-10 times a day) followed by 14 days without sucrose rinsing', 'armGroupLabels': ['Placebo', 'Probiotic']}]}, 'contactsLocationsModule': {'locations': [{'zip': '2200', 'city': 'Copenhagen', 'country': 'Denmark', 'facility': 'University of Copenhagen, Department of Odontology', 'geoPoint': {'lat': 55.67594, 'lon': 12.56553}}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'University of Copenhagen', 'class': 'OTHER'}, 'collaborators': [{'name': 'Deerland Probiotics and Enzymes', 'class': 'UNKNOWN'}], 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'DDS, PhD, Dr. odont', 'investigatorFullName': 'Daniel Belstrøm, DDS, PhD', 'investigatorAffiliation': 'University of Copenhagen'}}}}