{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Curarization%2C+Postoperative+Residual", "query": { "condition": "Curarization, Postoperative Residual" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 21, "total_pages": 3, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Curarization%2C+Postoperative+Residual&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-05-22T05:43:51.115Z", "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": "NCT03920670", "title": "Comparison of the ToFscan and TetraGraph During Recovery of Neuromuscular Function in the Post Anesthesia Care Unit", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Residual Neuromuscular Blockade" ], "interventions": [ { "name": "TetraGraph (TG)", "type": "DEVICE" }, { "name": "ToFscan (TS)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2019-02-28", "completion_date": "2020-11-30", "has_results": true, "last_update_posted_date": "2021-04-29", "last_synced_at": "2026-05-22T05:43:51.115Z", "location_count": 2, "location_summary": "Jacksonville, Florida • Evanston, Illinois", "locations": [ { "city": "Jacksonville", "state": "Florida" }, { "city": "Evanston", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03920670" }, { "nct_id": "NCT04352140", "title": "Electromyographic and Acceleromyographic Monitoring in Restricted Arm Movement Surgical Setting", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Residual Neuromuscular Blockade" ], "interventions": [ { "name": "Tetragraph", "type": "DEVICE" }, { "name": "ToFscan", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2020-08-18", "completion_date": "2022-02-14", "has_results": true, "last_update_posted_date": "2023-02-17", "last_synced_at": "2026-05-22T05:43:51.115Z", "location_count": 1, "location_summary": "Jacksonville, Florida", "locations": [ { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04352140" }, { "nct_id": "NCT04619225", "title": "Cardiac Output and Recovery Time", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Residual Neuromuscular Blockade" ], "interventions": [ { "name": "TetraGraph", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 7, "start_date": "2022-09-14", "completion_date": "2023-01-13", "has_results": true, "last_update_posted_date": "2026-02-04", "last_synced_at": "2026-05-22T05:43:51.115Z", "location_count": 1, "location_summary": "Jacksonville, Florida", "locations": [ { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04619225" }, { "nct_id": "NCT02728726", "title": "Sugammadex vs Placebo to Prevent Residual Neuromuscular Block", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "General Surgery" ], "interventions": [ { "name": "Sugammadex", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 260, "start_date": "2016-06", "completion_date": "2019-12", "has_results": true, "last_update_posted_date": "2022-07-14", "last_synced_at": "2026-05-22T05:43:51.115Z", "location_count": 2, "location_summary": "Jacksonville, Florida • Houston, Texas", "locations": [ { "city": "Jacksonville", "state": "Florida" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02728726" }, { "nct_id": "NCT03585348", "title": "Provider Variability in the Use of Neuromuscular Blocking Drugs and Reversal", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Neuromuscular Blockade", "Residual Curarisation, Postoperative", "Surgery Under General Anaesthesia" ], "interventions": [ { "name": "Neuromuscular blocking agents", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Beth Israel Deaconess Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 265537, "start_date": "2018-06-29", "completion_date": "2021-03-31", "has_results": false, "last_update_posted_date": "2021-08-25", "last_synced_at": "2026-05-22T05:43:51.115Z", "location_count": 2, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03585348" }, { "nct_id": "NCT02660398", "title": "Incidence and Severity of Residual Neuromuscular Blockade", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Residual Neuromuscular Blockade" ], "interventions": [ { "name": "Standardized NMBD Management", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 78, "start_date": "2016-01", "completion_date": "2017-01", "has_results": false, "last_update_posted_date": "2019-05-20", "last_synced_at": "2026-05-22T05:43:51.115Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT02660398" }, { "nct_id": "NCT02433808", "title": "Neostigmine Reversal And Neuromuscular Recovery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Residual Neuromuscular Block" ], "interventions": [ { "name": "Neostigmine Group", "type": "DRUG" }, { "name": "No Neostigmine group", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Endeavor Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 120, "start_date": "2015-04", "completion_date": "2017-04", "has_results": false, "last_update_posted_date": "2017-04-12", "last_synced_at": "2026-05-22T05:43:51.115Z", "location_count": 1, "location_summary": "Evanston, Illinois", "locations": [ { "city": "Evanston", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT02433808" }, { "nct_id": "NCT01545193", "title": "The Effect of Age on the Incidence of Postoperative Residual Neuromuscular Blockade", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Residual Neuromuscular Blockade in Elderly Patients" ], "interventions": [ { "name": "Age and incidence of residual neuromuscular blockade", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Endeavor Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 300, "start_date": "2011-06", "completion_date": "2014-09", "has_results": true, "last_update_posted_date": "2019-09-16", "last_synced_at": "2026-05-22T05:43:51.115Z", "location_count": 1, "location_summary": "Evanston, Illinois", "locations": [ { "city": "Evanston", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT01545193" }, { "nct_id": "NCT04352127", "title": "Visual and Electromyography Assessments in Response to Train-of-Four Stimulation of the Ulnar Nerve", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Residual Neuromuscular Blockade" ], "interventions": [ { "name": "TetraGraph", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 55, "start_date": "2020-08-18", "completion_date": "2021-06-29", "has_results": true, "last_update_posted_date": "2022-11-10", "last_synced_at": "2026-05-22T05:43:51.115Z", "location_count": 1, "location_summary": "Jacksonville, Florida", "locations": [ { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04352127" }, { "nct_id": "NCT02984839", "title": "Incidence of Residual Neuromuscular Blockade in Intra-abdominal Surgery: A Prospective, Observational Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Neuromuscular Blockade", "Pulmonary Complication" ], "interventions": [ { "name": "Stimpod NMS450® Nerve Stimulator, by Xavant™ Technology", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "OhioHealth", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2016-11", "completion_date": "2017-05-16", "has_results": false, "last_update_posted_date": "2018-07-26", "last_synced_at": "2026-05-22T05:43:51.115Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02984839" } ] }