Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D003924', 'term': 'Diabetes Mellitus, Type 2'}], 'ancestors': [{'id': 'D003920', 'term': 'Diabetes Mellitus'}, {'id': 'D044882', 'term': 'Glucose Metabolism Disorders'}, {'id': 'D008659', 'term': 'Metabolic Diseases'}, {'id': 'D009750', 'term': 'Nutritional and Metabolic Diseases'}, {'id': 'D004700', 'term': 'Endocrine System Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C000591245', 'term': 'semaglutide'}]}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'PROSPECTIVE', 'observationalModel': 'COHORT'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 789}, 'patientRegistry': False}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2020-02-13', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2023-03', 'completionDateStruct': {'date': '2021-05-25', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2023-03-24', 'studyFirstSubmitDate': '2020-02-06', 'studyFirstSubmitQcDate': '2020-02-06', 'lastUpdatePostDateStruct': {'date': '2023-03-28', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2020-02-10', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2021-05-25', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Change in Glycated Haemoglobin A1c (HbA1c)', 'timeFrame': 'Baseline (up to 12 weeks prior to treatment initiation (week 0) to end of study (week 28 to 38)', 'description': 'Percent point'}, {'measure': 'Change in HbA1c', 'timeFrame': 'Baseline (up to 12 weeks prior to treatment initiation (week 0) to end of study (week 28 to 38)', 'description': 'mmol/mol'}], 'secondaryOutcomes': [{'measure': 'Change in body weight (kg)', 'timeFrame': 'Baseline (up to 12 weeks prior to treatment initiation (week 0) to end of study (week 28 to 38)', 'description': 'kg'}, {'measure': 'Change in body weight (%)', 'timeFrame': 'Baseline (up to 12 weeks prior to treatment initiation (week 0) to end of study (week 28 to 38)', 'description': 'Percent'}, {'measure': 'Change in waist circumference', 'timeFrame': 'Baseline (up to 12 weeks prior to treatment initiation (week 0) to end of study (week 28 to 38)', 'description': 'cm'}, {'measure': 'HbA1c level below 8.0% (64 mmol/mol) (yes/no)', 'timeFrame': 'At end of study (week 28 to 38)', 'description': 'Number of participants'}, {'measure': 'HbA1c level below 7.5% (59 mmol/mol) (yes/no)', 'timeFrame': 'At end of study (week 28 to 38)', 'description': 'Number of participants'}, {'measure': 'HbA1c level below 7.0% (53 mmol/mol) (yes/no)', 'timeFrame': 'At end of study (week 28 to 38)', 'description': 'Number of participants'}, {'measure': 'Reduction in HbA1c of 1.0% point or more (yes/no)', 'timeFrame': 'Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38)', 'description': 'Number of participants who achieved/not achieved reduction in HbA1c of 1.0% point or more'}, {'measure': 'Weight reduction of 3.0% or more (yes/no)', 'timeFrame': 'Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38)', 'description': 'Number of participants who achieved/not achieved weight reduction of 3.0% or more'}, {'measure': 'Weight reduction of 5.0% or more (yes/no)', 'timeFrame': 'Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38)', 'description': 'Number of participants who achieved/not achieved weight reduction of 5.0% or more'}, {'measure': 'HbA1c reduction of 1.0% point or more and weight reduction of 3.0% or more (yes/no)', 'timeFrame': 'Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38)', 'description': 'Number of participants who achieved/not achieved HbA1c reduction of 1.0% point or more and weight reduction of 3.0% or more'}, {'measure': 'Patient reported severe or documented hypoglycaemia (yes/no)', 'timeFrame': 'Between baseline (week 0), end of study (week 28-38)', 'description': 'Count'}, {'measure': 'Change in score for Diabetes Treatment Satisfaction Questionnaire - Status (DTSQs) (absolute treatment satisfaction): Total treatment satisfaction', 'timeFrame': 'Baseline (week 0), end of study (week 28 to 38)', 'description': 'The status version (DTSQs) provides a measure of how satisfied patients are with their current diabetes treatment. It consists of 8 questions, which are to be answered on a Likert scale from 0 to 6 (0 = very dissatisfied to 6 = very satisfied). Six questions are summed to produce a total Treatment Satisfaction score. The remaining two questions are concerning perceived frequency of hyperglycaemia and perceived frequency of hypoglycaemia, respectively'}, {'measure': 'Change in score for Diabetes Treatment Satisfaction Questionnaire - Change (DTSQc) (relative treatment satisfaction): Total treatment satisfaction', 'timeFrame': 'Baseline (week 0), end of study (week 28 to 38)', 'description': 'The change version (DTSQc) has the same 8 items as the status version, but is reworded to direct the patients to compare the experience of the current treatment with the experience of previous treatment. Each question is scored on a scale of -3 to +3 (-3 = much less satisfied now to +3 = much more satisfied now), with 0 (midpoint), representing no change'}, {'measure': 'Change in score for Short Form (SF)-36 v2: Physical summary component', 'timeFrame': 'Baseline (week 0), end of study (week 28 to 38)', 'description': 'The SF-36®v2 questionnaire has 36 questions grouped into eight domains termed: physical functioning, bodily pain, role-physical, general health, vitality, social functioning, role-emotional and mental health, which again can be combined to give two summary component scores (overall mental- and physical health).'}, {'measure': 'Change in score for SF-36 v2: Mental summary component', 'timeFrame': 'Baseline (week 0), end of study (week 28 to 38)', 'description': 'The SF-36®v2 questionnaire has 36 questions grouped into eight domains termed: physical functioning, bodily pain, role-physical, general health, vitality, social functioning, role-emotional and mental health, which again can be combined to give two summary component scores (overall mental- and physical health).'}, {'measure': 'Patient completed the study under treatment with semaglutide (yes/no)', 'timeFrame': 'At end of study (week 28 to 38)', 'description': 'Count'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Diabetes Mellitus, Type 2']}, 'referencesModule': {'references': [{'pmid': '36809678', 'type': 'BACKGROUND', 'citation': 'Vilsboll T, Lindahl CO, Nielsen NF, Tikkanen CK. Real-world impact of once-weekly subcutaneous semaglutide after 2 years of follow-up: Results from a nationwide observational study in people with type 2 diabetes. Diabetes Obes Metab. 2023 Jun;25(6):1740-1749. doi: 10.1111/dom.15031. Epub 2023 Mar 9.'}]}, 'descriptionModule': {'briefSummary': 'The purpose of the study is to collect information on how semaglutide works in real world patients. Participants will get semaglutide prescribed by their study doctor. The study will last for about 6 to 8 months. The participants will be asked to complete some questionnaires about their health and their diabetes treatment. Participants will complete these during their normally scheduled visits with their study doctor.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'Participants with type 2 diabetes', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* \\- Signed informed consent obtained before any study-related activities (study-related activities are any procedures related to recording of data according to protocol)\n* The decision to initiate treatment with commercially available semaglutide has been made by the patient/Legally Acceptable Representative and the treating physician before and independently from the decision to include the patient in this study\n* Male or female, age 18 years or older at the time of signing informed consent\n* Diagnosed with type 2 diabetes at least 12 weeks prior to inclusion\n* Available and documented haemoglobin A1c (HbA1c) value equal to or below 12 weeks prior to initiation of semaglutide treatment\n\nExclusion Criteria:\n\n* \\- Previous participation in this study. Participation is defined as having given informed consent in this study\n* Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation\n* Treatment with any investigational drug within 90 days prior to enrolment into the study\n* Hypersensitivity to semaglutide or to any of the excipients'}, 'identificationModule': {'nctId': 'NCT04261933', 'acronym': 'SURE GERMANY', 'briefTitle': 'A Research Study Looking at How Semaglutide Works in People With Type 2 Diabetes in Germany, as Part of Local Clinical Practice (SURE GERMANY)', 'organization': {'class': 'INDUSTRY', 'fullName': 'Novo Nordisk A/S'}, 'officialTitle': 'A Multi-centre, Prospective, Noninterventional Study Investigating the Effectiveness of Once-weekly Subcutaneous Semaglutide in a Real World Adult Population With Type 2 Diabetes', 'orgStudyIdInfo': {'id': 'NN9535-4617'}, 'secondaryIdInfos': [{'id': 'U1111-1241-6291', 'type': 'OTHER', 'domain': 'World Health Organization (WHO)'}]}, 'armsInterventionsModule': {'armGroups': [{'label': 'Semaglutide s.c. once-weekly', 'description': "Participants will receive semaglutide at the treating physician's discretion as part of the usual clinical practice. The prescription and use of semaglutide is completely independent of this study. Total study duration for the individual patient will be approximately 30 weeks.", 'interventionNames': ['Drug: semaglutide']}], 'interventions': [{'name': 'semaglutide', 'type': 'DRUG', 'description': "Patients will be treated with commercially available semaglutide in a prefilled pen injector (FlexTouch® variant) according to routine local clinical practice at the discretion of the treating physician. 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