{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Pregnancy%2C+High-Risk&page=2", "query": { "condition": "Pregnancy, High-Risk", "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?condition=Pregnancy%2C+High-Risk&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-06-26T21:51:12.724Z", "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": "NCT01118351", "title": "Sunitinib Malate in Treating Patients With Recurrent Transitional Cell Bladder Cancer", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Recurrent Bladder Cancer", "Transitional Cell Carcinoma of the Bladder" ], "interventions": [ { "name": "sunitinib malate", "type": "DRUG" }, { "name": "immunohistochemistry staining method", "type": "OTHER" }, { "name": "TdT-mediated dUTP nick end labeling assay", "type": "OTHER" }, { "name": "light microscopy", "type": "OTHER" }, { "name": "laboratory biomarker analysis", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Case Comprehensive 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": 19, "start_date": "2008-10", "completion_date": "2015-09", "has_results": true, "last_update_posted_date": "2019-05-01", "last_synced_at": "2026-06-26T21:51:12.724Z", "location_count": 2, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" }, { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01118351" }, { "nct_id": "NCT03047369", "title": "The Myelin Disorders Biorepository Project", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Leukodystrophy", "White Matter Disease", "Leukoencephalopathies", "4H Syndrome", "Adrenoleukodystrophy", "AMN", "ALD", "ALD Gene Mutation", "ALD (Adrenoleukodystrophy)", "X-linked Adrenoleukodystrophy", "X-ALD", "Adrenomyeloneuropathy", "Aicardi Goutieres Syndrome", "AGS", "Alexander Disease", "Alexanders Leukodystrophy", "AxD", "ADLD", "Canavan Disease", "CTX", "Cerebrotendinous Xanthomatoses", "Krabbe Disease", "GALC Deficiency", "Globoid Leukodystrophy", "TUBB4A-Related Leukodystrophy", "H-ABC - Hypomyelination, Atrophy of Basal Ganglia and Cerebellum", "HBSL", "HBSL - Hypomyelination, Brain Stem, Spinal Cord, Leg Spasticity", "LBSL", "Leukoencephalopathy With Brain Stem and Spinal Cord Involvement and High Lactate Syndrome (Disorder)", "Leukoencephalopathy With Brainstem and Spinal Cord Involvement and Lactate Elevation", "ALSP", "CSF1R Gene Mutation", "HCC - Hypomyelination and Congenital Cataract", "MLC1", "Megalencephalic Leukoencephalopathy With Subcortical Cysts", "MLD", "Metachromatic Leukodystrophy", "PMD", "Pelizaeus-Merzbacher Disease", "PLP1 Null Syndrome", "PLP1 Gene Duplication | Blood or Tissue | Mutations", "Pelizaeus Merzbacher Like Disease", "Peroxisomal Biogenesis Disorder", "Zellweger Syndrome", "Refsum Disease", "Salla Disease", "Sialic Storage Disease", "Sjögren", "Sjogren-Larsson Syndrome", "Van Der Knapp Disease", "Vanishing White Matter Disease", "Charcot-Marie-Tooth", "CMT", "Mct8 (Slc16A2)-Specific Thyroid Hormone Cell Transporter Deficiency", "Allan-Herndon-Dudley Syndrome", "Cadasil", "Cockayne Syndrome", "Multiple Sulfatase Deficiency", "Gangliosidoses", "GM2 Gangliosidosis", "BPAN", "Labrune Syndrome", "LCC", "Mucopolysaccharidoses", "TBCK-Related Intellectual Disability Syndrome" ], "interventions": [], "intervention_types": [], "sponsor": "Children's Hospital of Philadelphia", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 12000, "start_date": "2016-12-08", "completion_date": "2030-12-08", "has_results": false, "last_update_posted_date": "2025-10-23", "last_synced_at": "2026-06-26T21:51:12.724Z", "location_count": 23, "location_summary": "Los Angeles, California • Orange, California • Palo Alto, California + 18 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Orange", "state": "California" }, { "city": "Palo Alto", "state": "California" }, { "city": "Sacramento", "state": "California" }, { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03047369" }, { "nct_id": "NCT03709004", "title": "Pacifiers and Breastfeeding Among Mothers at Risk for Postpartum Depression", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breastfeeding", "Postpartum Depression" ], "interventions": [ { "name": "Pacifier", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of California, Davis", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "12 Hours", "maximum_age": "45 Years", "sex": "ALL", "summary": "12 Hours to 45 Years" }, "enrollment_count": 0, "start_date": "2019-09-25", "completion_date": "2019-09-25", "has_results": false, "last_update_posted_date": "2019-09-27", "last_synced_at": "2026-06-26T21:51:12.724Z", "location_count": 1, "location_summary": "Sacramento, California", "locations": [ { "city": "Sacramento", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03709004" }, { "nct_id": "NCT06377878", "title": "The Preeclampsia Registry", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Preeclampsia", "Eclampsia", "HELLP Syndrome", "Toxemia", "Hypertensive Disorder of Pregnancy" ], "interventions": [], "intervention_types": [], "sponsor": "Preeclampsia Foundation", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "13 Years", "maximum_age": null, "sex": "ALL", "summary": "13 Years and older" }, "enrollment_count": 20000, "start_date": "2013-09-01", "completion_date": "2040-05", "has_results": false, "last_update_posted_date": "2024-04-22", "last_synced_at": "2026-06-26T21:51:12.724Z", "location_count": 1, "location_summary": "Melbourne, Florida", "locations": [ { "city": "Melbourne", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06377878" }, { "nct_id": "NCT00179816", "title": "Tandem Peripheral Blood Stem Cell (PBSC) Rescue for High Risk Solid Tumors", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Ewing's Sarcoma", "Soft Tissue Sarcoma", "Hepatoblastoma", "Hodgkin's Disease", "Germ Cell Tumor" ], "interventions": [ { "name": "High-Dose Chemotherapy with Tandem PBSC Rescue.", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Ann & Robert H Lurie Children's Hospital of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "21 Years", "sex": "ALL", "summary": "Up to 21 Years" }, "enrollment_count": 12, "start_date": "1999-04", "completion_date": "2012-09", "has_results": false, "last_update_posted_date": "2010-10-11", "last_synced_at": "2026-06-26T21:51:12.724Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT00179816" }, { "nct_id": "NCT05967806", "title": "A Study to Identify and Characterise Patients With Chronic Kidney Disease and Proteinuria", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Renal Disease" ], "interventions": [ { "name": "assessment", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "AstraZeneca", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "130 Years", "sex": "ALL", "summary": "18 Years to 130 Years" }, "enrollment_count": 2575, "start_date": "2023-07-31", "completion_date": "2024-08-30", "has_results": false, "last_update_posted_date": "2025-04-06", "last_synced_at": "2026-06-26T21:51:12.724Z", "location_count": 17, "location_summary": "Huntsville, Alabama • Bakersfield, California • Chatsworth, California + 14 more", "locations": [ { "city": "Huntsville", "state": "Alabama" }, { "city": "Bakersfield", "state": "California" }, { "city": "Chatsworth", "state": "California" }, { "city": "San Carlos", "state": "California" }, { "city": "South Gate", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05967806" }, { "nct_id": "NCT00776958", "title": "Lynne Cohen Consortium Project: Multi-Center Database/Registry", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Ovarian Cancer", "Breast Cancer" ], "interventions": [ { "name": "Questionnaire", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 176, "start_date": "2008-07", "completion_date": null, "has_results": false, "last_update_posted_date": "2014-07-31", "last_synced_at": "2026-06-26T21:51:12.724Z", "location_count": 4, "location_summary": "Birmingham, Alabama • Los Angeles, California • New York, New York + 1 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Los Angeles", "state": "California" }, { "city": "New York", "state": "New York" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00776958" }, { "nct_id": "NCT00994318", "title": "Ferric Carboxymaltose (FCM) Assessment in Subjects With Iron Deficiency Anaemia and Non-dialysis-dependent Chronic Kidney Disease (NDD-CKD)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Iron Deficiency Anaemia", "Chronic Kidney Disease" ], "interventions": [ { "name": "FCM (Ferric carboxymaltose) high ferritin target", "type": "DRUG" }, { "name": "FCM (Ferric carboxymaltose) low ferritin target", "type": "DRUG" }, { "name": "Oral Iron (Ferrous sulphate)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Vifor Pharma", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 626, "start_date": "2009-12", "completion_date": "2014-02", "has_results": true, "last_update_posted_date": "2014-05-20", "last_synced_at": "2026-06-26T21:51:12.724Z", "location_count": 1, "location_summary": "Wilmington, North Carolina", "locations": [ { "city": "Wilmington", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00994318" }, { "nct_id": "NCT07560813", "title": "NOURISH - A Healthcare-community Partnership to Improve Nutrition for Optimal Glycemic Control and Pregnancy Outcomes With Pregestational Diabetes", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Type 2 Diabetes", "Type 1 Diabetes", "Pregnancy, High Risk" ], "interventions": [ { "name": "Mid-Ohio Food Farmacy (MOF+) produce delivery", "type": "DIETARY_SUPPLEMENT" }, { "name": "Nutrition education with Dining with Diabetes (DWD)", "type": "BEHAVIORAL" }, { "name": "Health Impact Ohio Central Ohio Pathways Hub to address unmet social needs", "type": "BEHAVIORAL" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "BEHAVIORAL" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 174, "start_date": "2026-07-01", "completion_date": "2030-06-30", "has_results": false, "last_update_posted_date": "2026-06-22", "last_synced_at": "2026-06-26T21:51:12.724Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT07560813" }, { "nct_id": "NCT00687479", "title": "Insulin Action During Pregnancy in Woman at High Risk for Gestational Diabetes", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Gestational Diabetes Mellitus" ], "interventions": [], "intervention_types": [], "sponsor": "Woman's", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "42 Years", "sex": "FEMALE", "summary": "18 Years to 42 Years · Female only" }, "enrollment_count": 175, "start_date": "2006-01", "completion_date": "2009-12", "has_results": false, "last_update_posted_date": "2014-12-18", "last_synced_at": "2026-06-26T21:51:12.724Z", "location_count": 1, "location_summary": "Baton Rouge, Louisiana", "locations": [ { "city": "Baton Rouge", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT00687479" } ] }