diff --git a/src/test/resources/Issue593.json b/src/test/resources/Issue593.json index b3c82fe..213625a 100644 --- a/src/test/resources/Issue593.json +++ b/src/test/resources/Issue593.json @@ -1,189 +1,704 @@ { - "clinical_study": { - "brief_summary": { - "textblock": "CLEAR SYNERGY is an international multi center 2x2 randomized placebo controlled trial of" - }, - "brief_title": "CLEAR SYNERGY Neutrophil Substudy", - "overall_status": "Recruiting", - "eligibility": { - "study_pop": { - "textblock": "Patients who are randomized to the drug RCT portion of the CLEAR SYNERGY (OASIS 9) trial" + "success": true, + "error": null, + "response": [ + { + "loc": { + "long": 31.25, + "lat": 30.063 }, - "minimum_age": "19 Years", - "sampling_method": "Non-Probability Sample", - "gender": "All", - "criteria": { - "textblock": "Inclusion Criteria:" + "interval": "day", + "place": { + "name": "cairo", + "state": "qh", + "country": "eg" }, - "healthy_volunteers": "No", - "maximum_age": "110 Years" - 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"Assistant Professor of Medicine", - "investigator_full_name": "Binita Shah", - "investigator_affiliation": "NYU Langone Health" - }, - "study_first_submitted_qc": "March 12, 2019", - "start_date": { - "type": "Actual", - "content": "March 4, 2019" - }, - "has_expanded_access": "No", - "study_first_posted": { - "type": "Actual", - "content": "March 14, 2019" - }, - "arm_group": [ - { - "arm_group_label": "Colchicine" - }, - { - "arm_group_label": "Placebo" - } - ], - "primary_outcome": { - "measure": "soluble L-selectin", - "time_frame": "between baseline and 3 months", - "description": "Change in soluble L-selectin between baseline and 3 mo after STEMI in the placebo vs. colchicine groups." - }, - "secondary_outcome": [ - { - "measure": "Other soluble markers of neutrophil activity", - "time_frame": "between baseline and 3 months", - "description": "Other markers of neutrophil activity will be evaluated at baseline and 3 months after STEMI (myeloperoxidase, matrix metalloproteinase-9, neutrophil gelatinase-associated lipocalin, neutrophil elastase, intercellular/vascular cellular adhesion molecules)" - }, - { - "measure": "Markers of systemic inflammation", - "time_frame": "between baseline and 3 months", - "description": "Markers of systemic inflammation will be evaluated at baseline and 3 months after STEMI (high sensitive CRP, IL-1β)" - }, - { - "measure": "Neutrophil-driven responses that may further propagate injury", - "time_frame": "between baseline and 3 months", - "description": "Neutrophil-driven responses that may further propagate injury will be evaluated at baseline and 3 months after STEMI (neutrophil extracellular traps, neutrophil-derived microparticles)" - } - ], - "oversight_info": { - "is_fda_regulated_drug": "No", - "is_fda_regulated_device": "No", - "has_dmc": "No" - }, - "last_update_posted": { - "type": "Actual", - "content": "September 12, 2019" - }, - "id_info": { - "nct_id": "NCT03874338", - "org_study_id": "18-01323", - "secondary_id": "1R01HL146206" - }, - "enrollment": { - "type": "Anticipated", - "content": "670" - }, - "study_first_submitted": "March 12, 2019", - "condition": [ - "Neutrophils.Hypersegmented | Bld-Ser-Plas", - "STEMI - ST Elevation Myocardial Infarction" - ], - "study_type": "Observational", - "required_header": { - "download_date": "ClinicalTrials.gov processed this data on July 19, 2020", - "link_text": "Link to the current ClinicalTrials.gov record.", - "url": "https://clinicaltrials.gov/show/NCT03874338" - }, - "last_update_submitted": "September 10, 2019", - "completion_date": { - "type": "Anticipated", - "content": "February 1, 2022" - }, - "location": { - "contact": { - "phone": "646-501-9648", - "last_name": "Fatmira Curovic", - "email": "fatmira.curovic@nyumc.org" - }, - "facility": { - "address": { - "zip": "10016", - "country": "United States", - "city": "New York", - "state": "New York" - }, - "name": "NYU School of Medicine" - }, - "status": "Recruiting", - "contact_backup": { - "last_name": "Binita Shah, MD" - } - }, - "intervention": { - "intervention_type": "Drug", - "arm_group_label": [ - "Colchicine", - "Placebo" ], - "description": "Participants in the main CLEAR SYNERGY trial are randomized to colchicine/spironolactone versus placebo in a 2x2 factorial design. The substudy is interested in the evaluation of biospecimens obtained from patients in the colchicine vs placebo group.", - "intervention_name": "Colchicine Pill" - }, - "patient_data": { - "sharing_ipd": "No" - }, - "verification_date": "September 2019" - } + "profile": { + "tz": "Africa/Cairo", + "elevM": 23, + "elevFT": 75 + } + } + ] } \ No newline at end of file diff --git a/src/test/resources/Issue593.xml b/src/test/resources/Issue593.xml index bf78f3b..0c6c038 100644 --- a/src/test/resources/Issue593.xml +++ b/src/test/resources/Issue593.xml @@ -1,169 +1,691 @@ - - - - - ClinicalTrials.gov processed this data on July 19, 2020 - Link to the current ClinicalTrials.gov record. - https://clinicaltrials.gov/show/NCT03874338 - - - 18-01323 - 1R01HL146206 - NCT03874338 - - CLEAR SYNERGY Neutrophil Substudy - Studies on the Effects of Colchicine on Neutrophil Biology in Acute Myocardial Infarction: A Substudy of the CLEAR SYNERGY (OASIS 9) Trial - - - NYU Langone Health - Other - - - Population Health Research Institute - Other - - - National Heart, Lung, and Blood Institute (NHLBI) - NIH - - - NYU Langone Health - - No - No - No - - - - CLEAR SYNERGY is an international multi center 2x2 randomized placebo controlled trial of - - - Recruiting - March 4, 2019 - February 1, 2022 - February 1, 2021 - Observational - No - - Other - Prospective - - - soluble L-selectin - between baseline and 3 months - Change in soluble L-selectin between baseline and 3 mo after STEMI in the placebo vs. colchicine groups. - - - Other soluble markers of neutrophil activity - between baseline and 3 months - Other markers of neutrophil activity will be evaluated at baseline and 3 months after STEMI (myeloperoxidase, matrix metalloproteinase-9, neutrophil gelatinase-associated lipocalin, neutrophil elastase, intercellular/vascular cellular adhesion molecules) - - - Markers of systemic inflammation - between baseline and 3 months - Markers of systemic inflammation will be evaluated at baseline and 3 months after STEMI (high sensitive CRP, IL-1β) - - - Neutrophil-driven responses that may further propagate injury - between baseline and 3 months - Neutrophil-driven responses that may further propagate injury will be evaluated at baseline and 3 months after STEMI (neutrophil extracellular traps, neutrophil-derived microparticles) - - 2 - 670 - Neutrophils.Hypersegmented | Bld-Ser-Plas - STEMI - ST Elevation Myocardial Infarction - - Colchicine - - - Placebo - - - Drug - Colchicine Pill - Participants in the main CLEAR SYNERGY trial are randomized to colchicine/spironolactone versus placebo in a 2x2 factorial design. The substudy is interested in the evaluation of biospecimens obtained from patients in the colchicine vs placebo group. - Colchicine - Placebo - - - - - Patients who are randomized to the drug RCT portion of the CLEAR SYNERGY (OASIS 9) trial - - - Non-Probability Sample - - - Inclusion Criteria: - - - All - 19 Years - 110 Years - No - - - Binita Shah, MD - Principal Investigator - NYU School of Medicine - - - Fatmira Curovic - 646-501-9648 - fatmira.curovic@nyumc.org - - - Binita Shah, MD - - - - NYU School of Medicine -
- New York - New York - 10016 - United States -
-
- Recruiting - - Fatmira Curovic - 646-501-9648 - fatmira.curovic@nyumc.org - - - Binita Shah, MD - -
- - United States - - September 2019 - March 12, 2019 - March 12, 2019 - March 14, 2019 - September 10, 2019 - September 10, 2019 - September 12, 2019 - - Principal Investigator - NYU Langone Health - Binita Shah - Assistant Professor of Medicine - - - - Myocardial Infarction - ST Elevation Myocardial Infarction - Infarction - - - - Colchicine - - - No - - -
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