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164 studies match these filters. Showing 151–164 of 164 studies
| Registration number | Study | Status | Phase | Enrolment | Sites / countries | Start year | Last updated | Actions |
|---|---|---|---|---|---|---|---|---|
| NCT06455787 | J-Valve Transfemoral Pivotal Study The primary objective of this study is to assess the safety and efficacy of the J-Valve Transfemoral (TF) System in patients with symptomatic, severe (grade 3 or 4), native aortic valve regurgitation (AR) and AR-dominant mixed aortic valve disease, who are judged by a multi-disciplinary heart team t… ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 40 sites in total · contact listed | Recruiting | Not applicable | 194target | 40 / 5 | 2024 | May 4, 2026 | |
| NCT07209397 | Detrusor Nerve Radiofrequency Ablation for Overactive Bladder in Women The goal of this clinical trial is to learn if a vaginal radiofrequency (RF) device called MORPHEUSV works to treat overactive bladder (OAB) in women. Researchers also want to learn how safe the device is for this indication. This study will include women ages 22 to 80 who have had OAB symptoms for… ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 9 sites in total · contact listed | Recruiting | Not applicable | 202target | 9 / 1 | 2025 | Jan 30, 2026 | |
| NCT06122077 | Clinical Validation of Freenome Multiomics Blood Test for Lung Cancer Screening The PROACT LUNG study is a prospective multi-center observational study to validate a blood-based test for the early detection of lung cancer by collecting blood samples from high-risk participants who will undergo a routine, standard-of-care screening Low-Dose Computed Tomography (LDCT). ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 36 sites in total · contact listed | Recruiting | 20,000target | 36 / 1 | 2023 | Aug 5, 2025 | ||
| NCT06942949 | Evaluation of Enhanced Lithotripsy System (ELS) in the Treatment of Urinary Stones, A Pivotal Trial The purpose of this study is to evaluate the safety and performance of the ELS to treat urinary stones. The ELS is intended to break urinary stones into small fragments that can pass during or after the procedure with less or no discomfort. Eligible patients are male or females, age 21 or older, wit… ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 20 sites in total · contact listed | Recruiting | Not applicable | 101target | 20 / 1 | 2025 | Jun 16, 2026 | |
| NCT05862272 | A Phase 3B Study to Evaluate Bone Mineral Density With Long-Term Use of Relugolix Combination Tablet in Women With Uterine Fibroids or Endometriosis The purpose of this clinical trial to characterize changes in bone mineral density during continuous treatment with relugolix combination tablet for up to 48 months (4 years) and 1 year of post-treatment follow-up in premenopausal women with heavy menstrual bleeding associated with uterine leiomyoma… ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 120 sites in total | Recruiting | Phase 3 | 1,000target | 120 / 1 | 2023 | Aug 6, 2025 | |
| NCT04634240 | Staged Complete Revascularization for Coronary Artery Disease vs Medical Management Alone in Patients With AS Undergoing Transcatheter Aortic Valve Replacement Patients undergoing transcatheter aortic valve replacement (TAVR) often have concomitant coronary artery disease (CAD) which may adversely affect prognosis. There is uncertainty about the benefits and the optimal timing of revascularization for such patients. There is currently clinical equipoise re… ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 72 sites in total · contact listed | Recruiting | Not applicable | 4,000target | 72 / 2 | 2020 | Jul 24, 2025 | |
| NCT06190717 | Maturation of Arteriovenous Fistula With Automated Sonography Assessments Trial This is a prospective, multi-center, two-arm, randomized trial to quantify the performance of the EchoMark®/EchoSure® System for AVF diagnostic ultrasound when used under a protocol of biweekly use for assessing fistula maturation and reducing time to Clinical Maturation. ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 21 sites in total · contact listed | Recruiting | Not applicable | 304target | 21 / 1 | 2024 | Apr 13, 2026 | |
| NCT05561127 | Paclitaxel Coated Balloon for the Treatment of Chronic bEnigN sTricture- Bowel To determine the safety and efficacy of GIE Medical's ProTractX3™ TTS DCB for the treatment of recurrent benign bowel strictures. ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 33 sites in total · contact listed | Recruiting | Phase 3 | 171target | 33 / 1 | 2023 | Jun 25, 2025 | |
| NCT05561114 | Paclitaxel Coated Balloon for the Treatment of Chronic bEnigN sTricture- Esophagus To evaluate the safety and efficacy of the ProTractX3™ DCB for the treatment of benign esophageal strictures. ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 34 sites in total · contact listed | Recruiting | Phase 3 | 198target | 34 / 1 | 2023 | Jun 25, 2025 | |
| NCT05701358 | Physiology-guided vs Angiography-guided Non-culprit Lesion Complete Revascularization for Acute MI & Multivessel Disease COMPLETE-2 is a prospective, multi-centre, randomized controlled trial comparing a strategy of physiology-guided complete revascularization to angiography-guided complete revascularization in patients with acute ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardia… ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 113 sites in total · contact listed | Recruiting | Not applicable | 5,100target | 113 / 17 | 2023 | Jun 19, 2025 | |
| NCT05685433 | A Real World Study of eCoin for Urgency Urinary Incontinence: Post Approval Evaluation (RECIPE) A prospective, multicenter, single-arm study to evaluate the safety and effectiveness of the eCoin® implanted tibial nerve stimulator in subjects with urgency urinary incontinence (UUI). ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 22 sites in total · contact listed | Recruiting | Not applicable | 200target | 22 / 1 | 2023 | Jan 28, 2026 | |
| NCT06378632 | AN INTERNATIONAL, OBSERVATIONAL, BLINDED STUDY TO ASSESS THE PERFORMANCE OF THE CORDIO HEARO SYSTEM Study Design: This is an international, multicenter, observational, non-interventional, prospective, blinded, single-arm, two-period study, to collect patient utterances that will be retrospectively analyzed to determine the sensitivity and UPNR of the HearO system. ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 45 sites in total · contact listed | Recruiting | 500target | 45 / 3 | 2022 | Mar 26, 2025 | ||
| NCT05336240 | PCOM2 - The Physician Communication Intervention, Version 2.0 Poor quality of primary care providers' vaccine recommendations lead to low adolescent human papillomavirus vaccination rates and hundreds of thousands of adolescents unnecessarily at risk for HPV-associated cancers and diseases. Though a previous provider communication intervention, called PCOM, wa… ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 2 sites in total · contact listed | Recruiting | Not applicable | 120target | 2 / 1 | 2023 | Aug 26, 2024 | |
| NCT01574053 | Enroll -HD: A Prospective Registry Study in a Global Huntington's Disease Cohort Enroll-HD is a longitudinal, observational, multinational study that integrates two former Huntington's disease (HD) registries-REGISTRY in Europe, and COHORT in North America and Australasia-while also expanding to include sites in Latin America. More than 30,000 participants have now enrolled into… ✓ Contact✗ Claimed Nearest site: Wichita, Kansas, United States — 43 km away · 183 sites in total · contact listed | RecruitingNot verified since Feb 1, 2024 | 35,000target | 183 / 20 | 2012 | Feb 28, 2024 |