Jewel P-WCD Post-Approval Study (PAS)
NCT07256678 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 6330
Last updated 2025-12-01
Summary
The objective of this PAS is to demonstrate the continued safety and clinical effectiveness of the Jewel P-WCD.
Conditions
- Jewel-P WCD
Interventions
- OTHER
-
This study is an observational registry study of the Jewel P-WCD in post-market use
This study is an observational registry study of the Jewel P-WCD in post-market use
- OTHER
-
Jewel
This study is an observational registry study of the Jewel P-WCD in post-market use
Sponsors & Collaborators
-
Element Science, Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-01-31
- Primary Completion
- 2029-10-31
- Completion
- 2029-12-31
More Related Trials
-
Design Validation Hemodynamic Study of New Kendall SCD SmartFlow Compression System
NCT05945186 ·Status: UNKNOWN ·Phase: NA
-
Clinical Investigation for New Filter to Ostomy Bags
NCT01273038 ·Status: COMPLETED ·Phase: NA
-
COVID-19 Personal Protective Equipment for Vaccinated Health Workers and Convalescents
NCT06158724 ·Status: WITHDRAWN
-
Collection of Human Biological Samples for the Development and Validation of New Methods of Diagnosis and for the Realization of Expertises Diagnostics in the Field of Infectious Diseases and Tropical
NCT03912246 ·Status: COMPLETED ·Phase: NA
-
Evaluation of the Safety and Efficacy of Single-use Precision Filtered Infusion Sets for Intravenous Infusion
NCT04962516 ·Status: COMPLETED
-
Evaluate Retention of an Orally Administered Device Using Gamma Scintigraphy Study 2
NCT00780286 ·Status: COMPLETED ·Phase: PHASE1
-
A Device Study in Healthy Participants
NCT04848402 ·Status: COMPLETED ·Phase: PHASE1
-
Subcostal Temporary Extravascular Pacing IV (STEP IV) Study
NCT05457673 ·Status: COMPLETED ·Phase: NA
-
Optimizing Research Data Acquisition With Smart Pill Bottles
NCT06522698 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Béa Applicator and Béa Cervical Cap Safety and Usability Study
NCT05129553 ·Status: UNKNOWN ·Phase: NA
-
Suturable DuraGen™ PMCF Study
NCT04923867 ·Status: COMPLETED
-
Clinical Study Investigating Safety and Performance of a New Urinary Intermittent Catheter in Healthy Volunteers
NCT02965066 ·Status: COMPLETED ·Phase: NA
-
Longitudinal Trial Assessing Cellulite in Women Wearing a New Compression Garment
NCT05959681 ·Status: UNKNOWN ·Phase: NA
-
Pilot Safety Study to Determine the Ability of the Protector Cap Jet Injector to Prevent Cross-Contamination
NCT00219453 ·Status: COMPLETED ·Phase: PHASE1
-
Users Study Of The Caverject Delivery System
NCT01747928 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Monitoring of 5% Treatment Naïve Intravenous Immunoglobulin (IVIg) Primary Immunodeficiency Disease (PIDD) Patients Using the CareExchange® System: A Pilot Study Using 5% Gammaplex® IVIg in the Home Setting
NCT02176239 ·Status: COMPLETED
-
Generation of Positive Biological Samples to Epoetin for Doping Control.
NCT02920372 ·Status: COMPLETED ·Phase: PHASE1
-
OrganOx Metra® New Enrollment PAS
NCT05526326 ·Status: COMPLETED
-
Biologically Assisted Core Decompression of the Femoral Head Using the PerFuse Instrument and BioCUE
NCT02662881 ·Status: UNKNOWN
-
A 5 Year Clinical Investigation on Creos Xenoprotect
NCT02373787 ·Status: TERMINATED ·Phase: NA
-
Pivotal Study for Validation of Philips Dx (PDx)
NCT02529137 ·Status: COMPLETED
-
Evaluation of the Clinical Performance of the ZIKV Detect™ 2.0 IgM Capture ELISA
NCT03776903 ·Status: COMPLETED
-
Subcostal Temporary Extravascular Pacing V Study
NCT05633394 ·Status: COMPLETED ·Phase: NA
-
Manufacture of Clinical T-cell Products for Future Treatment
NCT05713513 ·Status: COMPLETED
-
Screening for Neonatal Jaundice With a Mobile Health Device: a Validation Study in Oaxaca, Mexico.
NCT06276582 ·Status: COMPLETED ·Phase: NA