{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Lumbar+spine+surgery", "query": { "intervention": "Lumbar spine surgery" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 155, "total_pages": 16, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Lumbar+spine+surgery&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-22T14:47:56.311Z", "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": "NCT03025256", "title": "Intravenous and Intrathecal Nivolumab in Treating Patients With Leptomeningeal Disease", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Acral Lentiginous Melanoma", "Central Nervous System Melanoma", "Clinical Stage IV Cutaneous Melanoma AJCC v8", "Leptomeningeal Neoplasm", "Melanocytoma", "Metastatic Lung Non-Small Cell Carcinoma", "Metastatic Melanoma", "Metastatic Mucosal Melanoma", "Metastatic Uveal Melanoma", "Stage IV Lung Cancer AJCC v8" ], "interventions": [ { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Lumbar Puncture", "type": "PROCEDURE" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Nivolumab", "type": "BIOLOGICAL" }, { "name": "Positron Emission Tomography", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "BIOLOGICAL" ], "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": 75, "start_date": "2018-05-02", "completion_date": "2027-06-01", "has_results": false, "last_update_posted_date": "2026-08-19", "last_synced_at": "2026-09-22T14:47:56.311Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03025256" }, { "nct_id": "NCT01861743", "title": "Multimodal Analgesia Versus Routine Care Pain Management", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Degenerative Disc Disease Lumbar", "Spinal Stenosis", "Lumbar Spondylolisthesis" ], "interventions": [ { "name": "Multimodal Analgesia", "type": "OTHER" }, { "name": "Patient controlled analgesia", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Rush University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 42, "start_date": "2013-04", "completion_date": "2017-12", "has_results": false, "last_update_posted_date": "2018-08-29", "last_synced_at": "2026-09-22T14:47:56.311Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT01861743" }, { "nct_id": "NCT02225444", "title": "A Prospective Study of Instrumented, Posterolateral Lumbar Fusions (PLF) With OsteoAMP®", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Spondylolisthesis", "Scoliosis", "Intervertebral Disc Disease" ], "interventions": [ { "name": "OsteoAMP", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Bioventus LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "21 Years to 85 Years" }, "enrollment_count": 42, "start_date": "2015-11-19", "completion_date": "2019-10-11", "has_results": false, "last_update_posted_date": "2020-11-05", "last_synced_at": "2026-09-22T14:47:56.311Z", "location_count": 9, "location_summary": "New Haven, Connecticut • Chicago, Illinois • Kansas City, Kansas + 6 more", "locations": [ { "city": "New Haven", "state": "Connecticut" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Kansas City", "state": "Kansas" }, { "city": "Paducah", "state": "Kentucky" }, { "city": "Royal Oak", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT02225444" }, { "nct_id": "NCT02674711", "title": "Study of Opioid Use After Lumbar and Cervical Spine Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Low Back Pain", "Opiate Addiction", "Neck Pain" ], "interventions": [ { "name": "Educational Video", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Brooke Army Medical Center", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 120, "start_date": "2015-08", "completion_date": "2018-06-01", "has_results": true, "last_update_posted_date": "2023-05-19", "last_synced_at": "2026-09-22T14:47:56.311Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02674711" }, { "nct_id": "NCT00927238", "title": "XL TDR® eXtreme Lateral Total Disc Replacement for the Treatment of Lumbar Degenerative Disc Disease (DDD)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Degenerative Disc Disease" ], "interventions": [ { "name": "XL TDR", "type": "DEVICE" }, { "name": "Lumbar fusion surgery", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "NuVasive", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 246, "start_date": "2009-07", "completion_date": "2015-07", "has_results": false, "last_update_posted_date": "2015-07-30", "last_synced_at": "2026-09-22T14:47:56.311Z", "location_count": 17, "location_summary": "Campbell, California • Thousand Oaks, California • Durango, Colorado + 14 more", "locations": [ { "city": "Campbell", "state": "California" }, { "city": "Thousand Oaks", "state": "California" }, { "city": "Durango", "state": "Colorado" }, { "city": "Newark", "state": "Delaware" }, { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT00927238" }, { "nct_id": "NCT03801356", "title": "Threshold Response of Lumbar Selective Nerve Root Block in Predicting Good Outcome Following Lumbar Foraminotomy", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Back Pain", "Radiculopathy Lumbar", "Degenerative Lumbar Spinal Stenosis" ], "interventions": [ { "name": "Selective Nerve Root Block", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 11, "start_date": "2018-08-23", "completion_date": "2020-12-15", "has_results": true, "last_update_posted_date": "2023-07-21", "last_synced_at": "2026-09-22T14:47:56.311Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03801356" }, { "nct_id": "NCT03688438", "title": "WoundVac in Obese Patients Undergoing Lumbar Surgery", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity", "Lumbar Spine Surgery" ], "interventions": [ { "name": "Closed-Incision Negative-Pressure Therapy", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Norton Leatherman Spine Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 124, "start_date": "2018-10-15", "completion_date": "2020-10-15", "has_results": false, "last_update_posted_date": "2018-09-28", "last_synced_at": "2026-09-22T14:47:56.311Z", "location_count": 1, "location_summary": "Louisville, Kentucky", "locations": [ { "city": "Louisville", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT03688438" }, { "nct_id": "NCT04584619", "title": "Idys™ TLIF 3DTi Post Market Clinical Follow-up", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Degenerative Disc Disease", "Grade 1 Spondylolisthesis" ], "interventions": [ { "name": "Spine fusion surgery with Clariance Idys TLIF 3DTi", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Clariance", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 25, "start_date": "2020-10-01", "completion_date": "2023-12-31", "has_results": false, "last_update_posted_date": "2021-11-29", "last_synced_at": "2026-09-22T14:47:56.311Z", "location_count": 1, "location_summary": "College Station, Texas", "locations": [ { "city": "College Station", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04584619" }, { "nct_id": "NCT03626246", "title": "Pathogenesis of Compromised Bone Quality and Mechanics in Chronic Kidney Disease", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Chronic Kidney Disease", "End Stage Kidney Disease", "Chronic Kidney Disease Mineral and Bone Disorder", "Renal Osteodystrophy", "Secondary Hyperparathyroidism" ], "interventions": [ { "name": "Kidney disease", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 50, "start_date": "2016-07-01", "completion_date": "2020-02-28", "has_results": false, "last_update_posted_date": "2021-07-13", "last_synced_at": "2026-09-22T14:47:56.311Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03626246" }, { "nct_id": "NCT01932983", "title": "Clinical Application of \"Train of Four\" Testing in the Intraoperative Monitoring Setting", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Neuromuscular Blockade", "Muscle Relaxation" ], "interventions": [ { "name": "Train of four test", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 150, "start_date": "2012-04", "completion_date": "2013-04", "has_results": false, "last_update_posted_date": "2015-10-27", "last_synced_at": "2026-09-22T14:47:56.311Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01932983" } ] }