{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+of+care+needle", "query": { "intervention": "Standard of care needle" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 217, "total_pages": 22, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+of+care+needle&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-14T15:08:48.797Z", "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": "NCT04544709", "title": "Intradiscal Platelet Rich Plasma", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Discogenic Pain", "Low Back Pain", "Chronic Pain" ], "interventions": [ { "name": "Low back intradiscal injection of platelet rich plasma (PRP)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 3, "start_date": "2019-02-14", "completion_date": "2022-07-29", "has_results": true, "last_update_posted_date": "2023-12-11", "last_synced_at": "2026-09-14T15:08:48.797Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT04544709" }, { "nct_id": "NCT01266044", "title": "Controlled Trial Of Acupuncture To Prevent Radiation-Induced Xerostomia", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Head And Neck Cancer" ], "interventions": [ { "name": "Acupuncture - Group 1", "type": "PROCEDURE" }, { "name": "Acupuncture - Group 2", "type": "PROCEDURE" }, { "name": "Standard Care", "type": "OTHER" }, { "name": "Questionnaire", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 435, "start_date": "2011-12-09", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-04-16", "last_synced_at": "2026-09-14T15:08:48.797Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01266044" }, { "nct_id": "NCT07221019", "title": "Single Shot Exparel vs Catheters in Lower Extremity Trauma", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Fracture Dislocation of Ankle Joint", "Fracture Leg", "Fracture Femur", "Fracture Lower Leg", "Fracture" ], "interventions": [ { "name": "Bupivacaine", "type": "DRUG" }, { "name": "Exparel + Bupivacaine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "George Washington University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 90, "start_date": "2025-09-12", "completion_date": "2029-08-11", "has_results": false, "last_update_posted_date": "2025-10-28", "last_synced_at": "2026-09-14T15:08:48.797Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07221019" }, { "nct_id": "NCT03152318", "title": "A Study of the Treatment of Recurrent Malignant Glioma With rQNestin34.5v.2", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Malignant Glioma of Brain", "Astrocytoma", "Malignant Astrocytoma", "Oligodendroglioma", "Anaplastic Oligodendroglioma of Brain (Diagnosis)", "Mixed Oligo-Astrocytoma", "Ependymoma", "Ganglioglioma", "Pylocytic/Pylomyxoid Astrocytoma", "Brain Tumor", "Glioma", "Brain Cancer", "Glioblastoma", "Glioblastoma Multiforme" ], "interventions": [ { "name": "rQNestin", "type": "DRUG" }, { "name": "Cyclophosphamide", "type": "DRUG" }, { "name": "Stereotactic biopsy", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "PROCEDURE" ], "sponsor": "Dana-Farber Cancer Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 62, "start_date": "2017-07-18", "completion_date": "2028-01", "has_results": false, "last_update_posted_date": "2026-03-04", "last_synced_at": "2026-09-14T15:08:48.797Z", "location_count": 5, "location_summary": "Baltimore, Maryland • Boston, Massachusetts • New York, New York + 1 more", "locations": [ { "city": "Baltimore", "state": "Maryland" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "New York", "state": "New York" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03152318" }, { "nct_id": "NCT04538417", "title": "C-RFA of Residual Limb Neuroma", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Phantom Limb Pain", "Neuroma Amputation" ], "interventions": [ { "name": "Cooled Radiofrequency Ablation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 8, "start_date": "2019-10-27", "completion_date": "2023-08-30", "has_results": true, "last_update_posted_date": "2025-01-08", "last_synced_at": "2026-09-14T15:08:48.797Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT04538417" }, { "nct_id": "NCT02681211", "title": "Auricular Acupuncture vs SOC in Migraine HA", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Migraine Headache" ], "interventions": [ { "name": "Auricular Acupuncture", "type": "OTHER" }, { "name": "Ketorolac 0.5mg/kg, max 30mg", "type": "DRUG" }, { "name": "Metoclopramide 0.1 mg/kg, max 10mg", "type": "DRUG" }, { "name": "Diphenhydramine 1mg/kg, max 50mg", "type": "DRUG" }, { "name": "Normal saline fluid bolus 20mL/kg, max 1000mL", "type": "DRUG" } ], "intervention_types": [ "OTHER", "DRUG" ], "sponsor": "University of Louisville", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "8 Years to 18 Years" }, "enrollment_count": 80, "start_date": "2016-02", "completion_date": "2024-11", "has_results": false, "last_update_posted_date": "2023-10-10", "last_synced_at": "2026-09-14T15:08:48.797Z", "location_count": 2, "location_summary": "Louisville, Kentucky", "locations": [ { "city": "Louisville", "state": "Kentucky" }, { "city": "Louisville", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT02681211" }, { "nct_id": "NCT05281731", "title": "Sonobiopsy for Noninvasive and Sensitive Detection of Glioblastoma", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Glioblastoma", "Glioblastoma Multiforme" ], "interventions": [ { "name": "Sonobiopsy", "type": "DEVICE" }, { "name": "Research blood", "type": "PROCEDURE" }, { "name": "Cancer Personalized Profiling", "type": "GENETIC" }, { "name": "Definity®", "type": "DEVICE" } ], "intervention_types": [ "DEVICE", "PROCEDURE", "GENETIC" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 40, "start_date": "2022-04-18", "completion_date": "2028-11-30", "has_results": false, "last_update_posted_date": "2026-05-14", "last_synced_at": "2026-09-14T15:08:48.797Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT05281731" }, { "nct_id": "NCT03322995", "title": "Pancreatic Cancer Adaptive Neoadjuvant Chemotherapy Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Pancreatic Cancer" ], "interventions": [ { "name": "First-line Chemotherapy", "type": "DRUG" }, { "name": "Second-line Chemotherapy", "type": "DRUG" }, { "name": "Chemoradiation", "type": "RADIATION" } ], "intervention_types": [ "DRUG", "RADIATION" ], "sponsor": "Medical College of Wisconsin", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 125, "start_date": "2018-06-21", "completion_date": "2032-06-01", "has_results": false, "last_update_posted_date": "2026-01-08", "last_synced_at": "2026-09-14T15:08:48.797Z", "location_count": 1, "location_summary": "Milwaukee, Wisconsin", "locations": [ { "city": "Milwaukee", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT03322995" }, { "nct_id": "NCT04003766", "title": "Endoscopic Ultrasound vs Percutaneous Route for Liver Biopsy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Liver Biopsy" ], "interventions": [ { "name": "biopsy", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "AdventHealth", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 40, "start_date": "2019-07-25", "completion_date": "2022-02-11", "has_results": false, "last_update_posted_date": "2022-02-24", "last_synced_at": "2026-09-14T15:08:48.797Z", "location_count": 1, "location_summary": "Orlando, Florida", "locations": [ { "city": "Orlando", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04003766" }, { "nct_id": "NCT03929783", "title": "Contrast Enhanced Mammography in Diagnosing Patients With Suspicious Breast Findings", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Neoplasms" ], "interventions": [ { "name": "Contrast Enhanced Digital Mammography", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Thomas Jefferson University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": "80 Years", "sex": "FEMALE", "summary": "30 Years to 80 Years · Female only" }, "enrollment_count": 107, "start_date": "2020-06-23", "completion_date": "2023-01-27", "has_results": false, "last_update_posted_date": "2025-04-29", "last_synced_at": "2026-09-14T15:08:48.797Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03929783" } ] }