{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Midline+Catheter&page=2", "query": { "intervention": "Midline Catheter", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Midline+Catheter&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-29T16:40:47.586Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT04811430", "title": "Efficiency, and Emergency Department Nurse Preference Between 2 Methods of Visualization: A Pilot Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Catheter Related Complication" ], "interventions": [ { "name": "Randomized Traditional", "type": "DEVICE" }, { "name": "Cue(TM) Needle Tracking Technology", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Becton, Dickinson and Company", "sponsor_class": "INDUSTRY", "healthy_volunteers": null, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 49, "start_date": "2019-10-14", "completion_date": "2019-10-15", "has_results": false, "last_update_posted_date": "2021-03-23", "last_synced_at": "2026-09-29T16:40:47.586Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04811430" }, { "nct_id": "NCT06632496", "title": "BD Prevue(TM) II Peripheral Vascular Access System With Cue(TM) Needle Tracking Technology Clinical Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "BD Prevue II for Peripheral Intravenous Catheter Placement" ], "interventions": [ { "name": "BD Prevue(TM) II", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Becton, Dickinson and Company", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Year", "maximum_age": null, "sex": "ALL", "summary": "1 Year and older" }, "enrollment_count": 156, "start_date": "2025-03-28", "completion_date": "2025-09-23", "has_results": false, "last_update_posted_date": "2026-01-16", "last_synced_at": "2026-09-29T16:40:47.586Z", "location_count": 2, "location_summary": "Brooklyn, New York • Pittsburgh, Pennsylvania", "locations": [ { "city": "Brooklyn", "state": "New York" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06632496" }, { "nct_id": "NCT02876055", "title": "Analgesic Efficacy of Interscalene Nerve Block Versus Local Infiltration Analgesia Following Total Shoulder Arthroplasty", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pain, Postoperative" ], "interventions": [ { "name": "Single shot interscalene nerve block", "type": "DRUG" }, { "name": "Continuous interscalene nerve block", "type": "DRUG" }, { "name": "Local Infiltration Analgesia (LIA)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 125, "start_date": "2016-11", "completion_date": "2018-02", "has_results": true, "last_update_posted_date": "2019-04-16", "last_synced_at": "2026-09-29T16:40:47.586Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT02876055" }, { "nct_id": "NCT06904911", "title": "Intra-Arterial Tenecteplase to Improve the Microvascular Hemodynamics After Mechanical Thrombectomy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Acute Ischemic Stroke From Large Vessel Occlusion" ], "interventions": [ { "name": "intra-arterial tenecteplase administration", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 20, "start_date": "2026-02-13", "completion_date": "2026-12-30", "has_results": false, "last_update_posted_date": "2026-08-18", "last_synced_at": "2026-09-29T16:40:47.586Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06904911" }, { "nct_id": "NCT06000787", "title": "MCT for the Harvard/UCSF ROBIN Center", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Glioma, Childhood Brainstem", "Neuroblastoma" ], "interventions": [ { "name": "External beam radiotherapy", "type": "RADIATION" }, { "name": "131I-Metaiodobenzylguanidine (MIBG)", "type": "RADIATION" } ], "intervention_types": [ "RADIATION" ], "sponsor": "Brigham and Women's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 47, "start_date": "2023-09-19", "completion_date": "2028-08-31", "has_results": false, "last_update_posted_date": "2025-02-17", "last_synced_at": "2026-09-29T16:40:47.586Z", "location_count": 2, "location_summary": "San Francisco, California • Boston, Massachusetts", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT06000787" }, { "nct_id": "NCT00706407", "title": "Uro-NIRS Clinical Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lower Urinary Tract Symptoms", "Overactive Bladder" ], "interventions": [ { "name": "Fully integrated Uro-NIRS:UDS", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Weill Medical College of Cornell University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 42, "start_date": "2008-04", "completion_date": "2010-05", "has_results": true, "last_update_posted_date": "2018-03-13", "last_synced_at": "2026-09-29T16:40:47.586Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00706407" }, { "nct_id": "NCT01881776", "title": "Continuous Interscalene Block Results in Superior Recovery Throughout the First Postoperative Week", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Postoperative Pain", "Adverse Effects" ], "interventions": [ { "name": "ISB", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "St. Luke's-Roosevelt Hospital Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 71, "start_date": "2011-08", "completion_date": "2012-06", "has_results": true, "last_update_posted_date": "2014-06-04", "last_synced_at": "2026-09-29T16:40:47.586Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01881776" }, { "nct_id": "NCT04264143", "title": "CED of MTX110 Newly Diagnosed Diffuse Midline Gliomas", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Diffuse Intrinsic Pontine Glioma", "Diffuse Pontine and Thalamic Gliomas", "Diffuse Midline Glioma" ], "interventions": [ { "name": "Infusate with MTX110 and gadolinium", "type": "DRUG" }, { "name": "Convection-Enhanced Delivery (CED)", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "DEVICE" ], "sponsor": "Luca Szalontay", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "3 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "3 Years to 18 Years" }, "enrollment_count": 9, "start_date": "2020-03-10", "completion_date": "2023-11-22", "has_results": false, "last_update_posted_date": "2023-12-18", "last_synced_at": "2026-09-29T16:40:47.586Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04264143" }, { "nct_id": "NCT07009678", "title": "Comparison of Lower vs Upper Extremity Injection Agitated Saline to Identify Patent Foramen Ovale With Echocardiography", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Patent Foramen Ovale", "Cryptogenic Stroke", "Embolic Infarction" ], "interventions": [ { "name": "intravenous access in greater saphenous vein compared to upper extremity site.", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "St. John's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 21, "start_date": "2023-03-01", "completion_date": "2025-05-12", "has_results": false, "last_update_posted_date": "2025-06-06", "last_synced_at": "2026-09-29T16:40:47.586Z", "location_count": 1, "location_summary": "Maple Grove, Minnesota", "locations": [ { "city": "Maple Grove", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT07009678" }, { "nct_id": "NCT06668766", "title": "Single Lumen Midline Catheter vs Long Peripheral Intravenous Cather for Difficult Intravenous Access in the ED", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Difficult Intravenous Access", "Midline Catheter", "Peripheral Intravenous Catheter", "Emergency Department Patient" ], "interventions": [ { "name": "10-cm Single Lumen Mildine", "type": "DEVICE" }, { "name": "4.78 cm Long Peripheral Intravenous Catheter", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Albany Medical College", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 270, "start_date": "2025-01-01", "completion_date": "2026-03-03", "has_results": false, "last_update_posted_date": "2026-08-25", "last_synced_at": "2026-09-29T16:40:47.586Z", "location_count": 1, "location_summary": "Albany, New York", "locations": [ { "city": "Albany", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06668766" } ] }