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164 studies match these filters. Showing 151–164 of 164 studies

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Registration numberStudyStatusPhaseEnrolmentSites / countriesStart yearLast updatedActions
NCT06455787J-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

RecruitingNot applicable194target40 / 52024May 4, 2026
NCT07209397Detrusor 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

RecruitingNot applicable202target9 / 12025Jan 30, 2026
NCT06122077Clinical 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

Recruiting20,000target36 / 12023Aug 5, 2025
NCT06942949Evaluation 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

RecruitingNot applicable101target20 / 12025Jun 16, 2026
NCT05862272A 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

RecruitingPhase 31,000target120 / 12023Aug 6, 2025
NCT04634240Staged 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

RecruitingNot applicable4,000target72 / 22020Jul 24, 2025
NCT06190717Maturation 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

RecruitingNot applicable304target21 / 12024Apr 13, 2026
NCT05561127Paclitaxel 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

RecruitingPhase 3171target33 / 12023Jun 25, 2025
NCT05561114Paclitaxel 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

RecruitingPhase 3198target34 / 12023Jun 25, 2025
NCT05701358Physiology-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

RecruitingNot applicable5,100target113 / 172023Jun 19, 2025
NCT05685433A 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

RecruitingNot applicable200target22 / 12023Jan 28, 2026
NCT06378632AN 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

Recruiting500target45 / 32022Mar 26, 2025
NCT05336240PCOM2 - 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

RecruitingNot applicable120target2 / 12023Aug 26, 2024
NCT01574053Enroll -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, 202435,000target183 / 202012Feb 28, 2024

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