Pilot Safety Study to Determine the Ability of the Protector Cap Jet Injector to Prevent Cross-Contamination
NCT00219453 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 17
Last updated 2007-04-19
Summary
The primary purpose of this study is to determine the ability of the Protector Cap Jet Injector to prevent cross-contamination in the next injection sample. The hypothesis is that the Protector Cap Jet Injector will prevent contamination in the next injection sample, even following injection of volunteers with high levels of hepatitis B virus.
Conditions
- Virus Diseases
- Hepatitis B
Interventions
- DEVICE
-
Jet Injector with Protector Cap (HSI-500)
Sponsors & Collaborators
-
Bill and Melinda Gates Foundation
collaborator OTHER -
PATH
lead OTHER
Principal Investigators
-
Darin L Zehrung, BS · PATH
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2004-10-31
- Completion
- 2006-01-31
More Related Trials
-
Manufacture of Clinical T-cell Products for Future Treatment
NCT05713513 ·Status: COMPLETED
-
Test Catheter Pilot Study in Healthy Volunteers
NCT00832078 ·Status: COMPLETED ·Phase: NA
-
Establishing Immunogenicity and Safety of Needle-free Intradermal Delivery of mRNA COVID-19 Vaccine
NCT05315362 ·Status: UNKNOWN ·Phase: PHASE2
-
Clinical Investigation to Evaluate the Hemanext® Red Blood Cell Processing System for Extended Storage of Leukoreduced Red Blood Cells
NCT04418934 ·Status: WITHDRAWN ·Phase: PHASE2
-
Blood Collection for Development and Validation of Point-of-Care Diagnostic Liver Function Tests
NCT05457543 ·Status: UNKNOWN
-
Continued Access Study to Evaluate Performance of the Organ Recovery Systems _LifePort® Liver Transporter System, a Machine Perfusion System, for Liver Transplant (PILOT™_CA)
NCT05574361 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Clinical Evaluation of the CM-1500 During Apheresis Blood Donation
NCT05012462 ·Status: COMPLETED ·Phase: NA
-
Evaluation of a Device That Separates Blood Cells From Serum/Plasma
NCT02853448 ·Status: COMPLETED ·Phase: NA
-
Safety Study of the Aethlon Hemopurifier
NCT02215902 ·Status: TERMINATED ·Phase: NA
-
Treatment of Long COVID Symptoms Utilizing Autologous Stem Cells Following COVID-19 Infection
NCT05669261 ·Status: UNKNOWN ·Phase: PHASE1
-
A Study to Assess Recovery and Survival of Radiolabeled Apheresis Platelet Components Treated With the INTERCEPT Blood System for Platelets With LED Illuminator.
NCT06697223 ·Status: COMPLETED ·Phase: PHASE2
-
Micro-hematology Analyzer for Viral/Bacterial Description
NCT05090319 ·Status: UNKNOWN
-
Users Study Of The Caverject Delivery System
NCT01747928 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Safety, Tolerability and Performance of the NucleoCapture Device in the Reduction of Circulating CfDNA/NETs in Subjects with Sepsis
NCT05647096 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Collection and Distribution of Blood Components From Healthy Donors for In Vitro Research Use
NCT00001846 ·Status: RECRUITING
-
COVID Card Pilot Study to Detect Antibodies to SARS-CoV-2
NCT05196932 ·Status: COMPLETED
-
Clinical Investigation of the Safety of the MediSieve Magnetic Haemofiltration System in Healthy Volunteers
NCT05713188 ·Status: COMPLETED ·Phase: PHASE1
-
A First-in-human Trial to Assess the Safety and Performance of the BioCaptis in Healthy Volunteers
NCT05813041 ·Status: UNKNOWN ·Phase: NA
-
Testing the Efficacy and Safety of the WEI Nasal Jet
NCT02005406 ·Status: COMPLETED
-
Long-Term Assessment of the Safety and Performance of the NuVasive Simplify Disc at Two Levels
NCT05691231 ·Status: ENROLLING_BY_INVITATION
-
Clinical Study Investigating Safety and Performance of a New Urinary Intermittent Catheter in Healthy Volunteers
NCT02965066 ·Status: COMPLETED ·Phase: NA
-
Clinical Investigation to Evaluate the Haemonetics POLFA Modified Sample Needle Assembly With Vacuum Tube Holder
NCT02476851 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Physiological Variables and Detection of Blood Loss Using the Zynex Fluid Monitoring System, Model CM-1600
NCT05463198 ·Status: COMPLETED ·Phase: NA
-
Evaluating the Analytical Equivalency of Serum and Whole Blood Samples Run on the MeMed Key® Platform (Perseverance Study)
NCT05439551 ·Status: COMPLETED
-
Blood Collection for Use in Serological Assay Development From Healthy Adult Volunteers
NCT00500032 ·Status: COMPLETED ·Phase: NA