A pilot study for chronic dialysis patients: Safety study using CV port and new needle for blood return of chronic dialysis patients

Phase 1

Recruiting

• Conditions: chronic dialysis patients, vascular access therapy; chronic dialysis patients, new vascular access therapy

• Registration Number: JPRN-jRCTs032200024
• Lead Sponsor: Yamagata Kunihiro

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-04-27
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 5

Inclusion Criteria

1) Chronic dialysis patients at participating institutions of this study
2) Patients who have difficulty in puncturing vascular access of arteriovenous fistula shunt, artificial graft, subcutaneously fixed superficial artery, or the autologous blood vessels, and are unable to secure an appropriate blood return, or can puncture but have insufficient blood return.
3) Men and women over 20 years old with written informed consent

Exclusion Criteria

1 participant allergic to CV port
2 If there is an infection at the CV port insertion site or if there is a suspicion of infection
3 participant with a cardiac pacemaker or ICD (implantable cardioverter defibrillator) in progress
4 participants who are judged inappropriate by the researcher
5 participants whose mean blood flow in maintenance dialysis are more than 210ml / min for 1 week just before study participation

Study & Design

• Study Type: Interventional
• Study Design: Not specified