Ignite Creation Date:
2025-12-25 @ 4:58 AM
Ignite Modification Date:
2025-12-26 @ 3:58 AM
Study NCT ID:
NCT05960318
Status:
COMPLETED
Last Update Posted:
2023-09-07
First Post:
2023-07-04
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Post Market Clinical Follow-Up Study - Medical Device KalobaNaso
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D003139', 'term': 'Common Cold'}, {'id': 'D012220', 'term': 'Rhinitis'}], 'ancestors': [{'id': 'D012141', 'term': 'Respiratory Tract Infections'}, {'id': 'D007239', 'term': 'Infections'}, {'id': 'D010850', 'term': 'Picornaviridae Infections'}, {'id': 'D012327', 'term': 'RNA Virus Infections'}, {'id': 'D014777', 'term': 'Virus Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}, {'id': 'D009668', 'term': 'Nose Diseases'}, {'id': 'D010038', 'term': 'Otorhinolaryngologic Diseases'}]}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'PROSPECTIVE', 'observationalModel': 'CASE_ONLY'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 131}, 'patientRegistry': False}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2023-05-08', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2023-09', 'completionDateStruct': {'date': '2023-07-31', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2023-09-06', 'studyFirstSubmitDate': '2023-07-04', 'studyFirstSubmitQcDate': '2023-07-21', 'lastUpdatePostDateStruct': {'date': '2023-09-07', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2023-07-25', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2023-07-31', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Resolution of the symptoms of nasal congestion', 'timeFrame': 'Before use and at the resolution (after maximum 7 days)', 'description': 'A 6-items close question questionnaire developed based on I-NOSE (Italian-Nose Obstruction Symptom Evaluation), a validated and published questionnaire. It is a five-points scale with values from 0 to 4 (0= not a problem; 4 = severe problem)'}], 'secondaryOutcomes': [{'measure': 'Rate of known and unknown side-effects and / or other risks associated to the use of medical device', 'timeFrame': 'During and after use (from the first application to after maximum 7 days)', 'description': 'Safety of the device during and after use'}]}, 'oversightModule': {'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Common Cold', 'Nasal Mucosal Inflammation', 'Rhinitis']}, 'descriptionModule': {'briefSummary': 'The goal of this observational PMCF study is to confirm the efficacy and safety of the medical device KalobaNaso (a nasal spray) in children, adolescents and adults with common cold symptoms, such as runny nose, nasal congestion and rhinitis. The main questions it aims to answer are:\n\n* Is the product effective in the treatment of common cold symptoms?\n* Is the product safe?\n\nAfter buying the product, participants will be asked to fill in a questionnaire, in order to:\n\n1. Assess the cold symptoms before the use of the nasal spray.\n2. Assess the resolution of cold symptoms after the use of the nasal spray.\n3. Describe the adverse effect(s)/problem(s) observed while using the product (if any).', 'detailedDescription': "The Medical Device Regulation (EU) 2017/745 (MDR) considers post-market clinical follow-up (PMCF) as a continuous process that aims to update the clinical evaluation and validate or reassess the benefit-risk balance of the medical device. The PMCF is an integral part of the manufacturer's post-market surveillance plan (PMS).\n\nThe medical device in question is CE marked since 2016, with no substantial modification.\n\nThe objectives of this Post Market Clinical Follow Up (PMCF) study are: verify the use of this device in a real situation, verify if its efficacy and safety of use are aligned with the provisions of the clinical evaluation; confirm or reassess the benefit/risk balance; update the risk analysis; identify any need for CAPA.\n\nSpecific product questionnaires have been developed based on the validated I-NOSE questionnaire, which aim to investigate aspects of Real-World Evidence on efficacy, safety, even in specific categories or situations, known and unknown adverse events, difficulties in use or completeness and clarity of IFUs.\n\nGiven the low-risk class of the device (class I - Dir.93/42/EEC), which is intended for use by lay people and normally sold in pharmacies / para-pharmacies, the sponsor planned to distribute the questionnaires to users that have purchased the product through health professionals (pharmacists), who are normally in charge of the distribution of the product.\n\nThe questionnaire was prepared in simple and easily understandable language for lay people.\n\nThe data requested during the filling of the questionnaire does not provide for the collection of information that allows the sponsor an identification of the participant.\n\nData will be collected and processed in a totally anonymous form."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT', 'OLDER_ADULT'], 'minimumAge': '2 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'Customers of the pharmacies/parapharmacies involved', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria adolescents ( \\> 12 years) and adults:\n\n* both sex, both smokers and not smokers, with symptoms of common cold, runny nose, nasal congestion, rhinitis, who bought the product by the pharmacy/parapharmacy involved.\n\nInclusion Criteria children (2 - 12 years old):\n\n\\- both sex, with symptoms of common cold, runny nose, nasal congestion, rhinitis, whose parents/caregivers bought the product by the pharmacy/parapharmacy involved\n\nExclusion Criteria adolescents (\\> 12 years) and adults:\n\n* children and adolescents under 12 years\n* Healthy volunteers and patients without symptoms associated to common cold, runny nose, nasal congestion, rhinitis,\n\nExclusion Criteria children (2-12 years old):\n\n* children \\< 2 years old\n* adolescents (\\>12 years old) and adults\n* Healthy volunteers and patients without symptoms associated to common cold, runny nose, nasal congestion, rhinitis,'}, 'identificationModule': {'nctId': 'NCT05960318', 'acronym': 'PMCF', 'briefTitle': 'Post Market Clinical Follow-Up Study - Medical Device KalobaNaso', 'organization': {'class': 'INDUSTRY', 'fullName': 'Schwabe Pharma Italia'}, 'officialTitle': 'Post Market Clinical Follow-Up Study on Medical Devices KalobaNaso Useful for Cold and Rhinitis in Adults and Children', 'orgStudyIdInfo': {'id': 'KN-01-2023'}}, 'armsInterventionsModule': {'armGroups': [{'label': 'Adolescents and adults', 'description': 'Adolescents from 12 years old and adults with common cold, nasal mucosa inflammation and/or rhinitis, who have bought the product.', 'interventionNames': ['Device: KalobaNaso spray']}, {'label': 'Children', 'description': 'Children from 2 to 12 years old with common cold, nasal mucosa inflammation and/or rhinitis, whose parents/caregivers have bought the product.', 'interventionNames': ['Device: KalobaNaso junior spray']}], 'interventions': [{'name': 'KalobaNaso spray', 'type': 'DEVICE', 'description': 'Nasal spray, 2 puff per nostril, 3 times a day', 'armGroupLabels': ['Adolescents and adults']}, {'name': 'KalobaNaso junior spray', 'type': 'DEVICE', 'description': 'Nasal spray, 1 puff per nostril, 3 times a day', 'armGroupLabels': ['Children']}]}, 'contactsLocationsModule': {'locations': [{'zip': '39044', 'city': 'Neumarkt', 'state': 'Bolzano', 'country': 'Italy', 'facility': 'Schwabe Pharma Italia', 'geoPoint': {'lat': 46.31777, 'lon': 11.27337}}], 'overallOfficials': [{'name': 'Floriana Raso', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Schwabe Pharma Italia'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Schwabe Pharma Italia', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}